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Boise - Regional Clinical Research Associate I/II

This is a home based regional Clinical Research Associate position. For this position you must have been with a pharmaceutical/Clinical Research Organization for at least six months. This must have clinical research associate experience. You must have independent monitoring experience. I will consider any therapeutic area. You must be within an hour of a major airport.

Boise - Veterinary Equipment Sales Rep

Worldwide leader of innovative technology-based products and services for the veterinary market seeks experienced sales rep. 2-5 year’s sales experience working for a manufacturer. Lab or medical equipment background preferred. Will look at veterinary candidates i.e. RVT, LVT etc. with a strong sales aptitude. Interested candidates please reply with updated resume.

Boone - Regional Clinical Research Associate, 70-90k

Please email your resume if you are interested in being contacted for an interview. Requirements: A minimum of 2 years experience as a regional CRA, more is better. 4 year degree 60 % travel 70-90K, outstanding benefits Thank-you for your time and interest!

Boone - Line Manager

PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, medical marketing and consulting services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Headquartered near Boston, Massachusetts, PAREXEL operates in 55 locations throughout 43 countries around the world, and has over 6,315 employees. For more information about PAREXEL International visit www.PAREXEL.com. Description: Responsible for organizing and managing all clinical data management activities on the company's largest and most complex projects including large teams and multiple protocols. Requires no supervision. Ability to solve problems using logical and systematic approaches is critical. Must thoroughly understand coding concepts, review of electronic data, medical encoding, SAE reconciliation and codebook applications. Must have solid understanding of therapeutic indications and study hypothesis. Acts as consultant with CDM's and teams for any and all data management issues and represents department at client meetings and presentations. Possesses in-depth knowledge in all areas of data management (coding, labs, SAE reconciliation, data validation manager, data validation specifications, tracking systems, Electronic Data Capture, or CRF Design). Makes recommendations for improvement of SOP's and WWP's resulting in streamlined processes and increased productivity. Experience: Education: BS/MS in health related or science discipline 2 year RN degree Minimum Work Requirements: Minimum of 4-8 years data management, clinical and/or research experience with solid understanding of clinical trials methodology and terminology Skills: Effectively applies technical knowledge to solve problems - Ability to provide advice or solutions based on expertise in technical areas to both internal groups and clients - Proactively seeks and takes action before being asked or the situation requires it - Ability to distinguish when an internal or external sign-off is necessary - Ability to determine when and how to escalate appropriate critical issues Offers support and constructive feedback to project team members please email resume to dorothy.hughes@parexel.com

Boone - Adventurous Biologists

Adventurous biologists to observe and sample catches onboard commercial fishing boats off Alaska. Duties include collecting representative samples of the catch, sorting, recording and measuring different species, Requires B.S. in biology or natural sciences, a college level statistics course and a flexible attitude. Strenuous working conditions. Opportunities year around. Training provided. While onboard fishing vessels, biologists identify fish species and collect and record data on the sex, length and quantity for species caught. This fishery data is used by government agencies such as National Marine Fisheries Service (NMFS) and Alaska Department of Fish and Game (ADF&G) to manage commercial fisheries. Requirements: Bachelor's Degree in fisheries science or other biological science, college level statistics course, pass a physical exam, and must have U.S. Citizenship. Please email your current resume to apply to yani@saltwaterinc.com and visit our website at www.saltwaterinc.com. Questions please call Yani at 907-276-3241.

Boston - All Around Office Person

All Around Office Person - with significant growth potential and excellent working conditions. Full time (min 30 hours) in Brookline Village (on the Green Line). Flexible hours could allow work only when school is in session. Includes excellent benefits – health insurance, life insurance, disability insurance, holidays etc. We would be pleased to employ a solid entry level candidate, a proven worker returning to the job market, or a “grey fox” older professional who for whatever reason (second thoughts about retirement?) would be interested in a new launch. Duties: mail and email distribution, receiving, packaging and shipping of products, filing, phone answering, light janitorial; willingness to do “what needs to be done” from A to Z in a small (7.5 person) office. If you can handle it, we can use you for customer service at all levels including technical sales. The more you can do the more you can get paid. Requirements: Excellent telephone intelligibility and computer skills and ability to learn quickly. Excellent telephone skills required. Must be pleasant and easy to work with. Beyond “required” – “desired” background (and more pay if you can supply and or all): skill in optics, biomedical optics, biophysics, biochemistry, computer network skills - or related background – grow into a more responsible position quickly. We are Boston Electronics Corporation, a 30 year old company specializing in photodetection, signal processing related to photodetection and related technologies. Our largest client base is biomedical/biophysical followed by industrial and aerospace. Compensation: $22K to 36K (or even more) depending on skills PS: If you saw our earlier advert October please respond again to this "sharpened" job description

Boston - Research Technician - Dana Farber Cancer Institute

Title:Research Technician Category:Lab Research and Sciences Requisition #:15409 Department:CB - Vidal Schedule:The hours of this position will vary to meet deadlines in order to complete experiments and achieve project goals in a timely fashion. Description: The Center for Cancer Systems Biology (CCSB) is currently seeking applications for a Research Technician to join the CCSB Human Interactome Project. The major duties are to work with Group Leaders and Staff Scientists to carry out high throughput yeast two-hybrid screening, recombinational cloning and microbial transformations as part of a large-scale protein interaction mapping project for both humans and model organisms. Responsibilities will involve all steps of protein interaction mapping using yeast two hybrid systems, including preparation of media, perform screening assays, maintaining strains and microbial stocks, along with other lab duties such as providing help to other ongoing projects in the lab, supplies ordering, managing resources and maintaining liquid handling systems. The hours of this position will vary to meet deadlines in order to complete experiments and achieve project goals in a timely fashion. Requirements: BS degree, or equivalent, with at least 1 to 2 years previous laboratory experience required. Must have hands on experience with preparation of microbial media, agarose gel electrophoresis, PCR, molecular biology, and microbiology. Experience with either mammalian cell culture and transfection, with robotic liquid handling systems, and/or with yeast two-hybrid assays is highly desirable. Please Apply here: http://www.dana-farber.org/abo/working/open/job_detail.asp?jobID=15409

Boulder - Senior Manager / Associate Director Clinical Research-cPharmaceutical

Senior Manager / Associate Director Clinical Research-cPharmaceuticalReference #: C-SP-1-172 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). BS/BA in a relevant scientific discipline plus a minimum of 6 years of relevant clinical experience or life science environment in the pharmaceutical industry or equivalent. Clinical research experience in phase I – III oncology clinical trials (preferred). Previous experience in managing regional contract monitors or CROs (highly desired). A strong knowledge of GCP and/or ICH guidelines, regulatory requirements & quality assurance procedures. Ability to write protocols, study reports, sections for the Investigator’s Brochure & regulatory documents (e.g. IND, NDA, etc.) with some supervision. Ability to collaborate with the contracts administrator to issue requests for proposal (RFPs), select contract research organizations (CROs)/Vendors/Contract CRAs & manage vendors/CROs & contractors throughout the clinical trial process. The ability to effectively problem solve & use clear judgment relating to national & international regulations, guidelines, investigator interaction & project timelines. Proficiency with Microsoft Office Suite. Position may require up to 20% travel. Job Description: Support the clinical research department in overall planning & implementation of oncology development studies, project deliverables, budgets & timelines. May manage multiple projects/assignments at any given time. Managing & providing oversight of clinical operations deliverables for assigned studies including management of staff who are performing monitoring visits for evaluation & selection of sites, study initiation, data collection, source data verification, clinical drug supply accountability & review of regulatory documents/files. Partnering with the head of clinical operations in planning the program budgets & timelines as well as managing the overall quality of project deliverables. Coordinating and/or participating in a leadership role in Investigator Meetings, clinical team meetings & ongoing training to internal team & external team (including study coordinators, investigators, & vendors regarding company processes). Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 136 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Boulder - Asbestos/Industrial Hygiene Professional

Job Description: Asbestos/Industrial Hygiene Professional Full-time position. Stewart Environmental Consultants, Inc. is a 20-year-old Fort Collins, Colorado-based team of engineers and scientists that provides environmental engineering, industrial hygiene, and laboratory testing services. This position reports to Stewart’s Environmental Services department manager. This position will support several new long-term contracts that will include asbestos surveys, asbestos abatement design and project management, asbestos abatement clearance services, indoor air quality surveys, mold investigations, methamphetamine lab investigations, and other industrial hygiene services. This position will assist the department manager with project management, including multi-phase asbestos abatement projects developed and executed in conjunction with client architects and general contractors. A critical function for this position will be the ability to develop plans and specifications for asbestos abatement design and assist with management of abatement projects. The candidate may also assist junior staff with field assignments, including abatement observations and clearance services, during peak times. The candidate should have 5 to 7 years of experience performing asbestos surveys for school and non-school projects and for abatement project designs. Good writing skills are preferred, as the candidate will prepare written reports, proposals, and specifications. Good organizational skills will be crucial to managing multiple tasks and projects, schedules. Education/Experience/Certifications: •Must have current AHERA-level asbestos inspector training and annual refreshers and must possess or have the ability to obtain a current Colorado Asbestos Building Inspector/Management Planner license. •Must have current Colorado Air Monitoring Specialist training or equivalent professional training certificates and refreshers and either possess or have the ability to obtain a Colorado Air Monitoring Specialist license; NIOSH PCM training preferred but not required •Candidate will possess or have the ability to obtain Colorado Asbestos Project Designer license. •Associates degree or higher preferred, including courses in Science, Environmental Studies, Engineering, Industrial Hygiene, and Health & Safety. •Experience preparing cost estimates and written proposals preferred. •Work well with other people as a team player, but also capable of working independently. •Project management experience highly valued. •Valid driver’s license and acceptable driving record. •Experience with methamphetamine lab surveys a plus. •OSHA HAZWOPER a plus.

Bgky - Regional Clinical Research Associate, 70-90k

Please email your resume if you are interested in being contacted for an interview. Requirements: A minimum of 2 years experience as a regional CRA, more is better. 4 year degree 60 % travel 70-90K, outstanding benefits Thank-you for your time and interest!

Brownsville - Lab Assistant - PT/FT in Bayview

We are a cosmetic manufacturing company in Bayview TX. We are looking for a lab assitant. Please fax your resume to 956-233-1890, call at 956-233-5001 or email to mbockelman@sarati.com The applicant will assists in the overall smooth running of the R & D Department and all of its functions. Job Duties: Wash dishes & general lab cleanup Maintain MSDS & COA documentation on all raw materials Inventory of Samples Stocked Manage Stability Testing (Make sure all new products have had stability tests run & passed, documentation of testing included in R & D files) Assist in-house R & D projects (make samples in lab) Assist in Private Label R & D projects (make samples in lab) Be flexible to learn new duties (packaging, shipping, technical, etc) Duties and responsibilities are subject to change upon business needs

Buffalo - LABORATORY - LAB TECHS

Antech Diagnostics, part of VCA Antech, Inc., is the largest provider of veterinary related services in the United States. Antech Diagnostics operates over 30 laboratories throughout the country servicing over 15,000 animal hospitals in all 50 states, making it the largest provider of outsource diagnostic services. We are currently seeking Laboratory Technicians for our Tampa, FL location. Ideal candidate will have general lab experience. Microbiology, Hematology and Chemistry experience is desirable. We offer standard medical, dental, vision care benefits, 401(k), life insurance, and pet healthcare discounts too.

Buffalo - Regional Clinical Research Associate, 70-90k

Please email your resume if you are interested in being contacted for an interview. Requirements: A minimum of 2 years experience as a regional CRA, more is better. 4 year degree 60 % travel 70-90K, outstanding benefits Thank-you for your time and interest!

Buffalo - Field Service Technician

Field Service Technician Precision Scale & Balance has what people want! Great employees, great environment and great culture. We are a leader in providing scale and laboratory balance maintenance, calibration, installation, and support. If you are seeking outstanding career opportunities and the chance to be a part of a strong team, this is the place for you. Job duties and responsibilities include: • Responding to emergency service calls • Installation of new equipment, maintenance, and calibration of Laboratory and Industrial Weighing equipment. Requirements:• Two year degree in electronics or equivalent experience required. • Highly motivated individual who can work alone or with a team. • Strong written and oral communication skills. Computer skills required. • Knowledge of ISO and 17205 requirements a plus. • Must have valid NYS driver’s. Some overnight travel. Vehicle provided. Benefits package includes health insurance, 401K, & paid vacation. Send resume and salary requirements to: Precision Scale & Balance 140 Rotech Drive Lancaster, NY 14086 or Fax to: 716-759-3931 or Email to: employment@scaleandbalance.com

Buffalo - Scientist Job - Clarence, NY

Scientist Job - Clarence, NYApply for this Scientist Job in Clarence HERE!Division: Medical PowerPosition: ScientistRequirements: . Ph.D. with more than 3 years of research experience in Lithium and Li-ion batteries preferred. . Demonstrated computer skills and instrumentation skills as stated by accountabilities. Strong oral and written skills that also includes problem solving and the ability to work in a team environment. . Experience with design of experiments (DOE) is a plus.Description: Greatbatch is seeking a Senior R&D Scientist for material and battery research. This position will plan, conduct and direct research and development projects where the complexity of the technical problems requires advanced knowledge in material science and electrochemistry. Industrial experience with battery material research is required with demonstrated problem solving and hands-on laboratory skills. Experience with Lithium and Li-Ion batteries is necessary. You will need to have a strong background in material analysis and possess solid fundamental understanding of chemical and electrochemical principles in battery research. Familiarity of analytical techniques such as XRD, SEM, Impedance Spectroscopy and DSC is a must. This position will also be responsible for writing proposals, reports, plans and presenting technical papers to enhance and promote the Greatbatch, Inc. image. Reviews technical and patent issues and has patent responsibility.Explore other Engineering Jobs in Buffalo HERE!

Buffalo - Medication Management Systems Specialist

Aspire to achieve greatness. Greatness starts with an individual dream and is realized through action and determination to be the best. At Hospira, our vision of Advancing Wellness™ through the right people and the right products is achieved each day by more than 14,000. Our sales organization makes a significant contribution to the success of our organization by educating our customers about how our products directly address key issues they face including: providing the very best patient care, enhancing patient and healthcare worker safety, improving productivity, and targeting cost containment and reduction. We seek talented sales pros driven to be part of a team of dedicated, customer-focused individuals who aspire to excel in all that they do. Medication Management Systems Specialist In this role you will supply hospitals with IV medication management infusion device systems. Key clients will include materials management, purchasing, information technology, and nursing. You will also establish strong business relationships, influence decision-makers, monitor and assess the competitive environment, achieve territory sales goals and manage territory expenses. Your territory will be central New York. To be successful in this position, you must possess: BS/BA degree 2-5+ years capital equipment and software sales experience Travel will be required Successful sales background Project management and contract negotiations Information technology/wireless experience Clinical/Nursing is preferred with pain management/infusion pump experience Our people make Hospira an organization of stature, and we’re proud of our accomplishments. We deliver on our commitment to our communities through charitable partnerships, thoughtful giving, product donations, and global relief. We foster a culture of respect, we value integrity above all, and we empower employees to own ideas and be accountable for actions. And we reward performance with diverse avenues for growth, superior education and training, and the types of benefits you’d expect from a market leader. What do you aspire? Look closely at the work you do and consider the impact you can make at Hospira. Learn more and apply online, visit: https://sjobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?jobId=123291&type=search&JobReqLang=1&recordstart=1&JobSiteId=5100&JobSiteInfo=123291_5100&partnerid=16015&siteid=5100 Req #: 4463BR As an equal opportunity/affirmative action employer, Hospira embraces diversity of thought and cultural perspective and fosters an environment of empowerment, fairness and respect.

Buffalo - Medication Management Systems Specialist

Aspire to achieve greatness. Greatness starts with an individual dream and is realized through action and determination to be the best. At Hospira, our vision of Advancing Wellness™ through the right people and the right products is achieved each day by more than 14,000. Our sales organization makes a significant contribution to the success of our organization by educating our customers about how our products directly address key issues they face including: providing the very best patient care, enhancing patient and healthcare worker safety, improving productivity, and targeting cost containment and reduction. We seek talented sales pros driven to be part of a team of dedicated, customer-focused individuals who aspire to excel in all that they do. Medication Management Systems Specialist In this role you will supply hospitals with IV medication management infusion device systems. Key clients will include materials management, purchasing, information technology, and nursing. You will also establish strong business relationships, influence decision-makers, monitor and assess the competitive environment, achieve territory sales goals and manage territory expenses. Your territory will be central New York. To be successful in this position, you must possess: BS/BA degree 2-5+ years capital equipment and software sales experience Travel will be required Successful sales background Project management and contract negotiations Information technology/wireless experience Clinical/Nursing is preferred with pain management/infusion pump experience Our people make Hospira an organization of stature, and we’re proud of our accomplishments. We deliver on our commitment to our communities through charitable partnerships, thoughtful giving, product donations, and global relief. We foster a culture of respect, we value integrity above all, and we empower employees to own ideas and be accountable for actions. And we reward performance with diverse avenues for growth, superior education and training, and the types of benefits you’d expect from a market leader. What do you aspire? Look closely at the work you do and consider the impact you can make at Hospira. Learn more and apply online, visit: https://sjobs.brassring.com/1033/ASP/TG/cim_jobdetail.asp?jobId=123291&type=search&JobReqLang=1&recordstart=1&JobSiteId=5100&JobSiteInfo=123291_5100&partnerid=16015&siteid=5100 Req #: 4463BR As an equal opportunity/affirmative action employer, Hospira embraces diversity of thought and cultural perspective and fosters an environment of empowerment, fairness and respect.

Buffalo - Regional Clinical Research Associate I/II

This is a home based regional Clinical Research Associate position. For this position you must have been with a pharmaceutical/Clinical Research Organization for at least six months. This must have clinical research associate experience. You must have independent monitoring experience. I will consider any therapeutic area. You must be within an hour of a major airport.

Buffalo - If I Were You I Would Do This NOW!7993877

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Buffalo - Laboratory Supply & Chemical Sales

Laboratory Sales Representative Expand your professional options. Build your own client base. We are looking for experienced scientific and chemical sales professionals who know the meaning of relationship sales and believe in taking care of customers. Do you call on labs, research, QC/QA, manufacturing or clinical labs? Are you limited to what you can sell and make? This is a well paying commission opportunity allowing the right person a part time or a full time option. No cap on the income you can earn. We are distributor of laboratory supplies, consumables and chemicals providing reps the flexibility of managing their business. If you understand this market and know how to convert competitive products, this can be a great opportunity for you. Requirements: BS Degree: chemistry, bio-related or equivalent Understanding market and customer needs Maintain updated knowledge of the industry and competitor’s products Prepare sales contract, contracts, quotes, prices and terms Four plus years sales experience Computer skills: Web, excel & word Independent Organized Responsible Dependable Demonstrate growth and profitability Simple formula for success: Build the business profitably and ethically Do not waste selling time with management reports, weekly plans or useless busy-reports The customer is number one! This is a commission only opportunity. Email: labrep@yahoo.com

Buffalo - Adventurous Biologists

Adventurous biologists to observe and sample catches onboard commercial fishing boats off Alaska. Duties include collecting representative samples of the catch, sorting, recording and measuring different species, Requires B.S. in biology or natural sciences, a college level statistics course and a flexible attitude. Strenuous working conditions. Opportunities year around. Training provided. While onboard fishing vessels, biologists identify fish species and collect and record data on the sex, length and quantity for species caught. This fishery data is used by government agencies such as National Marine Fisheries Service (NMFS) and Alaska Department of Fish and Game (ADF&G) to manage commercial fisheries. Requirements: Bachelor's Degree in fisheries science or other biological science, college level statistics course, pass a physical exam, and must have U.S. Citizenship. Please email your current resume to apply to yani@saltwaterinc.com and visit our website at www.saltwaterinc.com. Questions please call Yani at 907-276-3241.

Capecod - Regulatory Operations Manager/Associate Director

Regulatory Operations Manager/Associate Director Our client is a global biotechnology company committed to the discovery and development of breakthrough small molecule drugs for serious diseases. The Company’s strategy is to commercialize its products both independently and in collaboration with major pharmaceutical companies. Their product pipeline is focused on viral diseases, inflammation, autoimmune diseases, cancer, pain and bacterial infections Responsibilities: •Regulatory Operations Manager/Associate Director will manage the operational activities around regulatory submissions across programs. •The individual will oversee routine submissions and lead operational coordination of submissions. •In addition, the individual is responsible to develop and maintain expertise in relevant topics to ensure quality and compliance for activities within the scope of their role. •Managerial responsibilities include work performance oversight and technical and personal development of direct reports. Requirements: •Qualified candidates will have a BS/BA in Life Sciences, Business Administration, Information Technology or related field •5-8 years of relevant work experience in pharmaceutical/biotech industry, preferably Regulatory Operations or Regulatory Affairs. •Candidate must demonstrate expertise in ICH eCTD and global regulatory submission practices and demonstrate competence in a supervisory role. •This individual must be highly-organized and able to effectively multi-task, possess excellent communication and negotiation skills, posses project management skills. •We are seeking an individual who is committed to innovation and able to lead others in a changing environment. This position is located in Cambridge, MA Once you choose to join the exciting team at this renowned company, you will be rewarded with a competitive salary and full benefits. Apply today to recruiting@fuzehr.com – www.fuzehr.com Thank you for your application, however only chosen candidates will be contacted. ** If you are not currently in the market for a new job, but know someone who could benefit from this opportunity, please don’t hesitate to forward this information, thank you.

Capecod - Facility Operator

John Todd Ecological Design, Inc., located in Woods Hole, MA hereinafter referred to as JTED, is currently seeking a qualified Grade 4-M licensed operator for the daily operations of a 27,500 gpd Eco-Machine™ located in Ipswich, MA. The wastewater treatment system uses living plants in aquatic tanks, along with a subsurface flow wetland and UV disinfection for treatment. Job responsibilities will include working closely with JTED staff, along with the maintenance staff for the owner of the treatment facility, to ensure the plant’s proper operation. This is a full time job, 8 a.m. to 4:30 p.m., which sometimes includes weekend work and being on-call for emergencies. Operational responsibility includes, but is not limited, to the following: 1) Sampling of monitoring wells and wastewater using composite samplers, Quanta systems, peristaltic pumps, and proper record keeping techniques. 2) Testing and monitoring the water on-site for Alkalinity, pH, Ammonia, DO, Nitrate, and Settleability 3) Backwashing sandfilters, housekeeping, vegetation care, giving tours, cleaning and repairing an Ultraviolet Disinfection unit, and other misc. tasks 4) Preparing weekly reports for JTED along with Monthly, Quarterly, and Semi-Annual reports for the Massachusetts DEP Must provide your own transportation to and from work, have good math and computer skills, and write well. Knowledge of extended aeration and RAS systems a plus. JTED is willing to train the right candidate. Interested applicants can send their resume by e-mail to andrew@toddecological.com or by mail to JTED, 87 Water Street, PO Box 497, Woods Hole, MA 02543. You may also call with questions at 978 380-7449.

Capecod - Clinical Pharmacologist

If you or someone you know has any interest in the position below please forward your resume as a word format attachment. Requirements: PharmD, PhD or MD degree preferred with several years of relevant clinical and pharmaceutical industry experience in the planning and conducting of clinical trials (involvement in non-clinical trials a plus). 0-5 years clinical pharmacology and pharmacokinetics experience, including development of clinical pharmacology programs for new chemical entities. Experience directing clinical (and non-clinical) pharmacology studies and preparation of regulatory submissions. Extensive knowledge of pharmacokinetic and pharmacodynamic principles. Experience interacting with regulatory authorities on Clinical Pharmacology/ Pharmacokinetic issues. Experience with advanced data analysis skills. Notes and Comments: Responsibilities: Develop clinical pharmacology plans, design and direct clinical pharmacology studies. Work with Study Logistics, CROs and other vendors to execute clinical pharmacology studies. Will design clinical pharmacology studies and in conjunction with Study Logistics be responsible for protocol development, study implementation, analysis and reporting of results. Will be responsible for clinical pharmacology sections of Investigator Brochures, IND, CTD and other regulatory submissions. Responsible and accountable of the clinical pharmacology components of drug development. Preparation of relevant documentation, as well as high-quality evaluation and interpretation of clinical pharmacology data (pharmacokinetics, pharmacodynamics, safety, dose/concentration response) from clinical studies. Provide thoughtful interpretation of the PK/PD data obtained for the entire development program/s. Interaction and response to regulatory agencies. Thank you & hope to hear form you soon,

Capecod - DIRECTOR OF R+D

DIRECTOR OF R AND D The Director of Research and Development oversees and directs the design, development, test and support of medical devices and associated systems. Manages and oversees the project management and provides technical guidance for a variety of cross functional activities. Supervises mentors and provides leadership to subordinate software, biology and engineering staff assigned to project(s). Responsible for initiation and completion of cross functional projects. Works on complex technical problems where analysis of situations or data requires an in-depth evaluation of various factors. Directs and coordinates all activities necessary to complete a major mechanical design project, design modification or several immediate projects. Serves as liaison on specific projects between functional departments. ESSENTIAL JOB FUNCTIONS AND RESPONSIBILITIES Defines and ensures implementation of multiple new product development plans and programs for the division reporting to the CTO of the company. Monitors smooth execution of plans and programs at lower levels and cross-functionally. Ensures proper allocation of resources to achieve project goals within established timelines and budgets. Develops a passion and working knowledge related to medical devices that enables effective judgment (design decisions, interaction with key customers, supervision of technical design reviews, engagement and "brainstorming" with multiple constituents including marketing, etc). Works interactively with peer group in R&D as well as managers, Directors and VP's of Quality, Operations, Regulatory, Marketing, Finance and Business Development. A general working knowledge of manufacturing strategy is a plus. Responsible for communications (as appropriate) to senior management. Individual must be able to communicate technical and non-technical information effectively to all levels of internal and external stakeholders. Individual must be a champion for innovation and people development working to strengthen the overall engineering team for both managerial and technical tracks. Responsible for managing multi-site relationships including both direct and indirect reports (as appropriate). Must be able to travel to support internal employees and external customers. Works within R&D to support strategies aimed at optimizing all phases of the product development cycle ensuring design quality, compliance to regulatory / industry standards, and customer satisfaction. Makes recommendations to streamline and to increase robustness of the new product development process. Ensures adherence to design control guidelines and regulatory compliance requirements. Collaborates closely with Engineering, Marketing, Manufacturing, and Finance to analyze market needs and potential business opportunities. OTHER RESPONSIBILITIES Coordinates with other departments such as manufacturing engineering, quality, materials, customer service and marketing to analyze and resolve problems. Ensure schedules are well planned and followed. Supervise and coordinate activities of assigned engineers, technicians and contractors. Provide technical guidance, leadership, goal-setting, communications and facilitation skills as needed to guide and motivate project personnel. Assure appropriate training and skill development is furnished to project staff as needed. Provide input to company strategic and long-range business plan, and ensure that development projects further those goals. Negotiate with other development staff and company departments to resolve conflicts and bottlenecks affecting projects. Responsible for compliance with Good Laboratory Practices, international compliance standards and company procedures. JOB KNOWLEDGE, SKILLS AND ABILITIESA doctorate degree (PhD or MD) in a scientific discipline, medical technology or equivalent. A strong background in Prenatal or Oncology Should have 5+ years of industry experience in developing medical/biological measurement devices. Demonstrated success in product development and bringing concepts to market. Consistent, proven leadership experience. The individual must possess initiative and focus to drive complete projects from the development stage through manufacturing and commercialization. Requires excellent written and verbal communication skills and the ability to work with individuals from all departments within the organization. Must have good computer skills, project management, word processing, database management, and spreadsheets. SUPERVISORY RESPONSIBILITIESDirectly oversees the management of 3-10 scientists and technicians. Guides the groups basic research and development goals Oversees individuals in all departments related to product development

Capecod - SCIENTIST PROJECT LEADER

LAB SCIENTIST PROJECT LEADER The Project Leader oversees and directs the design and development of new applications for medical devices and associated systems. Manages and oversees the project management and provides technical guidance for specific projects. Works with software, biology and engineering staff assigned to project(s). Responsible for initiation and completion of specific projects. Works on complex technical problems where analysis of situations or data requires an in-depth evaluation of various factors. Leads activities necessary to complete the development of a specific product. Serves as liaison on specific projects between functional departments. ESSENTIAL JOB FUNCTIONS AND RESPONSIBILITIES Defines and ensures implementation of multiple new product development plans and programs for the division reporting to the Director of R&D. Monitors smooth execution of design and development plans and programs at lower levels. Ensures proper allocation of resources to achieve project goals within established timelines and budgets. Develops a passion and working knowledge related to medical devices that enables effective judgment (design decisions, interaction with key customers, supervision of technical design reviews, engagement and "brainstorming" with multiple constituents including marketing, etc). Works interactively with peer group in R&D as well as managers, Directors and VP's of Quality, Operations, Regulatory, Marketing, Finance and Business Development. Responsible for communications (as appropriate) to senior management. Individual must be able to communicate technical and non-technical information effectively to all levels of internal and external stakeholders. Individual must be a champion for innovation and people development working to strengthen the overall engineering team for both managerial and technical tracks. Responsible for managing both direct and indirect reports (as appropriate). Must be able to travel to support internal employees and external customers. Works within R&D to support strategies aimed at optimizing all phases of the product development cycle ensuring design quality, compliance to regulatory / industry standards, and customer satisfaction. Makes recommendations to streamline and to increase robustness of the new product development process. Ensures adherence to design control guidelines and regulatory compliance requirements. Collaborates closely with Engineering, Marketing, Manufacturing, and Finance to analyze market needs and potential business opportunities. OTHER RESPONSIBILITIES Coordinates within R&D and with collaborators to analyze and resolve problems. Ensure schedules are well planned and followed. Supervise and coordinate activities of assigned engineers, technicians and contractors. Provide technical guidance, leadership, goal-setting, communications and facilitation skills as needed to guide and motivate project personnel. Assure appropriate training and skill development is furnished to project staff as needed. Provide input to company strategic and long-range business plan, and ensure that development projects further those goals. Negotiate with other development staff and company departments to resolve conflicts and bottlenecks affecting projects. Responsible for compliance with Good Laboratory Practices, international compliance standards and company procedures. JOB KNOWLEDGE, SKILLS AND ABILITIES A doctorate degree (PhD or MD) in a scientific discipline, medical technology or equivalent. Should have 3+ years of industry experience in developing medical/biological measurement devices. Experience in product development. Consistent, proven leadership experience. The individual must possess initiative and focus to drive complete projects from the development stage through manufacturing and commercialization. Requires excellent written and verbal communication skills and the ability to work with individuals from all departments within the organization. Must have good computer skills, project management, word processing, database management, and spreadsheets. Experience in FISH staining SUPERVISORY RESPONSIBILITIES Directly oversees the management of 2-5 scientists and technicians. Guides a research and development team towards product development Oversees individuals in the group assigned for a specific project(s)

Capecod - Oceanographer/Programmer Needed

PROGRAMMER NEEDED at Fisheries in Woods Hole to provide assistance in the development of a sea turtle bycatch model across fishery gear types, specifically by preparing satellite remotely sensed data and ocean model data to serve as input into the modeling process. Send Resume to HR@integratedstatistics.com OBJECTIVES AND BACKGROUND Under the Endangered Species Act, the National Marine Fisheries Service is required to assess the status of the bycatch of non-target species by commercial fisheries in U.S. waters. The Protected Species Branch (PSB) of the Northeast Fisheries Science Center carries out the responsibilities of the NMFS in the northeast region with the PSB responsible for regular assessments of the bycatch of sea turtles. To estimate the number of sea turtle interactions, separate bycatch estimates are currently prepared for several fisheries. The objective of this contract is to support modeling of sea turtle interactions with multiple fisheries using remotely sensed environmental data and regional ocean models (ROMs). Results of this study could streamline the bycatch estimation process and facilitate informative management decisions with inferred sea turtle distribution and habitat. REQUIREMENTS The primary responsibilities shall be to provide assistance in the preparation of remotely sensed satellite and ocean model data to serve as input into the sea turtle bycatch modeling process. Also, to provide assistance writing programs that streamline the acquisition, processing, and distribution of satellite data for use in protected species bycatch and habitat research. Examples of processing satellite data include automating downloading of sea surface temperature (SST) satellite images, creation multi-day SST image composites, and distribution of SST images with custom tools to merge the data to fisheries datasets. Additional duties may include (but not be limited to) developing and disseminating custom GIS tools for fisheries scientist use, preparing fisheries datasets for analysis, performing statistical analyses, and assisting in the calculation of the sea turtle bycatch model. The individual may be required to present findings, as necessary, at professional meetings and participate in Branch field operations to gain a better understanding of the data being utilized. Minimum qualifications of contractor personnel are as follows: Bachelors degree or higher in biological science with quantitative coursework Programming skills and experience with IDL or Matlab, ArcGIS, databases (Oracle/SQL or MS Access), and statistical software (SAS, Splus, or R) Familiarity with satellite oceanography Ability to present study results in written and oral forms Ability to function in a team environment and to produce under defined time constraints Desirable qualities of the contracted personnel include: Knowledge of Northwest Atlantic Ocean sea turtle distribution and ecology Experience with VB, VBA, Python, or similar programming language used to create custom GIS tools

Capecod - Facility Operator

John Todd Ecological Design, Inc., located in Woods Hole, MA hereinafter referred to as JTED, is currently seeking a qualified Grade 4-M licensed operator for the daily operations of a 27,500 gpd Eco-Machine™ located in Ipswich, MA. The wastewater treatment system uses living plants in aquatic tanks, along with a subsurface flow wetland and UV disinfection for treatment. Job responsibilities will include working closely with JTED staff, along with the maintenance staff for the owner of the treatment facility, to ensure the plant’s proper operation. This is a full time job, 8 a.m. to 4:30 p.m., which sometimes includes weekend work and being on-call for emergencies. Operational responsibility includes, but is not limited, to the following: 1) Sampling of monitoring wells and wastewater using composite samplers, Quanta systems, peristaltic pumps, and proper record keeping techniques. 2) Testing and monitoring the water on-site for Alkalinity, pH, Ammonia, DO, Nitrate, and Settleability 3) Backwashing sandfilters, housekeeping, vegetation care, giving tours, cleaning and repairing an Ultraviolet Disinfection unit, and other misc. tasks 4) Preparing weekly reports for JTED along with Monthly, Quarterly, and Semi-Annual reports for the Massachusetts DEP Must provide your own transportation to and from work, have good math and computer skills, and write well. Knowledge of extended aeration and RAS systems a plus. JTED is willing to train the right candidate. Interested applicants can send their resume by e-mail to andrew@toddecological.com or by mail to JTED, 87 Water Street, PO Box 497, Woods Hole, MA 02543. You may also call with questions at 978 380-7449.

Capecod - Environmental Biology Technician

Environmental Biology Technician Working in the Ecotoxicology department, working with different cultures, organisms, invertebrates and fish. Maintaining chemical/aquarium systems, observing different fish and plant species for exposure to chemical compounds in development. Working with different reagents and solvents. Care and maintenance of fish populations, recording of observations and data. Some repetitive work, occasional weekend work. Education/Requirements: Minimum of High School diploma or Associate's degree in a Science related field. Some experience with laboratory techniques required. Commonwealth Sciences, Inc. http://www.cwsciences.com Please apply with a resume to laureno@cwsciences.com

Carbondale - Project Engineer

Hexion Specialty Chemicals is the world's largest producer of thermosetting resins. The second-largest North American-based specialty chemicals Company. Hexion generated 2006 sales of $5.2 billion through its leading positions across various end markets and geographies. Our resins are used in bonding, binding and coating applications in a multitude of industries and for virtually thousands of end-use products. Our materials are found in products touching nearly every modern living. Job Objective: Provide long term capital planning process to support Site Mission - reliability manufacture quality products in a safe and environmentally compliant manner to meet business strategies. Essential Functions: Perform preliminary engineering to identify critical project requirements, develop alternatives, conduct cost/benefit analysis to prioritize options, anticipate issues, bottlenecks and roadblocks, develop scope and documents to conduct project reviews, and recommend best options to management. Achieve best return on capital by managing project budget, schedule and performance to meet key performance requirements at the lowest overall manufacturing cost (considering capital, M&R and operating). Perform detailed engineering to develop project scopes/packages that meet critical project requirements, including budget, schedule and performance. Project packages shall support operations, maintainability, constructability, safety and permit reviews. Provide documentation for all engineering and process design, to include equipment and piping drawings, specifications, calculations and analysis, including basis. Understand and meet PSM requirements for engineering and process design. Use MOC process for changes. Understand and meet other regulatory requirements for engineering design, installation and constructions. Provide management with accurate and timely information with which to make justified and appropriate decisions. Make recommendations and await required approval of projects, and spending. Understand regulatory & permit requirements, and obtain required documents in a timely basis by providing necessary information. Obtain required permits for procurement, installation and construction in a timely and efficient manner. Support SMLT contractor management strategy by forecasting workload, provide project design packages for best project controls & change management, communicate and review packages with all stakeholders. Education/Experience - Bachelors Degree in Technical Area (Highly prefer Chemical Engineering) - Ideal candidate will have 5 - 10 years of Project Engineering experience (Highly prefer in Chemical Industry) - Computer skills - Excellent communication both verbal and written - Leadership - Strong Technical Knowledge - Process Safety Management and Process Hazard Analysis To learn more about this and other exciting opportunities with Hexion, visit www.hexion.com to search for jobs and view detailed job descriptions. To Apply for this position, please CLICK HERE

Catskills - *** MARKETING AGENTS WANTED ***6487133

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Catskills - Adventurous Biologists

Adventurous biologists to observe and sample catches onboard commercial fishing boats off Alaska. Duties include collecting representative samples of the catch, sorting, recording and measuring different species, Requires B.S. in biology or natural sciences, a college level statistics course and a flexible attitude. Strenuous working conditions. Opportunities year around. Training provided. While onboard fishing vessels, biologists identify fish species and collect and record data on the sex, length and quantity for species caught. This fishery data is used by government agencies such as National Marine Fisheries Service (NMFS) and Alaska Department of Fish and Game (ADF&G) to manage commercial fisheries. Requirements: Bachelor's Degree in fisheries science or other biological science, college level statistics course, pass a physical exam, and must have U.S. Citizenship. Please email your current resume to apply to yani@saltwaterinc.com and visit our website at www.saltwaterinc.com. Questions please call Yani at 907-276-3241.

Cnj - Im looking to get into the Bio Careers

I am looking to get into the biohazardous materials career, specificly crime scen clean up. Is there a company that will hire & train you??? If any one has any information, please reply,Thank You.

Cnj - Director, Clinical Operations

We are a Princeton located start up pharmaceutical development and clinical research company with operations in India. The founder of this company has identified pharmaceutical contract research and clinical research services to be a significant business opportunity to be sourced out of India, which is becoming a major hub for pharmaceutical R & D and Clinical research. The company's clients are small to medium sized US pharmaceuticals who could take advantage of lower developmental costs and large pool of patient population in India. To exploit this opportunity, the company is largely using research, regulatory, analytical and clinical resources out of India and intellectual property, project & operations management and business development resources in the USA. To structure these operations, the company has a fully functional Indian affiliate in Mumbai. To achieve the company's business objectives, the founder is looking for a highly motivated entrepreneurial Director, Clinical Operations to pilot the program acquisition and management and ensure service delivery. Position; Director, Clinical Operations The Director, Clinical Operations reports and assists the President of the company in achieving business objectives. He will lead a team of Program/Project Managers and is responsible for leading the design, management and execution of all of company’s clinical projects and to achieve client satisfaction levels. The Director must have the vision, experience, and personal stature to be able to create, communicate and execute the vision of the clinical research program operations. The person needs to have EXCELLENT clinical trials management and people management skills, late phase experience though very desirable, but not required. Knowledge of/experience with CRO processes and NBD experience is preferred. We are open to varied therapeutic areas expertise. He would Manage and oversee the project management and provide technical guidance for a variety of cross functional activities. He will supervise, mentor and provide leadership to clinical operations team across India and US. Responsible for initiation, completion and deliver scheduled timely results of cross functional projects. Experience /skills • Must be an entrepreneurial oriented to contribute and grow with a start up • Must have a Ph D or MD in the medical or life sciences; • Eight –ten years clinical research experience with a minimum of four years hand on management of clinical research programs • Clinical Research experience from Phase 1 through Phase 3 is required. He or she need not have taken a single product through each step sequentially, but must have the experience and skills necessary to help lead the entire clinical development process. • Good understanding of the clinical development process/GCPs/ICH guidelines • Knowledge in multiple therapeutic areas preferable • Computer literacy in MS Word, MS Project, Power Point and Excel and excellent presentation skills • Effective communication (verbal and written) and organizational skills • Excellent interpersonal skills and Proactive approach • Must be willing to travel a minimum of 20% domestically and/or internationally as required. Compensation and Benefits The founder is looking for someone with capabilities to grow, with the company, into the position of chief operating officer of the clinical research busness. Compensation is very competitive with very high bonus potential. Other benefits include medical and dental coverage and paid vacation. Contact Please email your resume to set up a meeting.

Cnj - Manager, Biostatistics (Nonclinical/Preclinical)-cPharmaceutical

Manager, Biostatistics (Nonclinical/Preclinical)-cPharmaceuticalReference #: C-EE-11-240 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). Education or education/experience combination equivalent to a post graduate degree in statistics or statistics related field. At least 4 years of pharmaceutical experience with a Ph.D. or Ph.D. equivalent. At least 6 years of pharmaceutical experience with a masters degree or masters degree equivalent. At least 3 years of experience with PK/PD analyses by quantitative modeling & simulation. Statistical leadership in early phase drug development with pre clinical & phase I/II studies. Statistical expertise with regard to clinical & pre clinical studies in Methodology; analysis of variance, mixed linear models, mixed non linear models, Bayesian analysis, trial simulation, compartmental modeling, categorical data analysis, reliability, multivariate analysis, robust estimation, nonparametric techniques. Statistical expertise with regard to clinical & pre clinical studies in Analysis; individual, average, & population PK analyses, bioequivalence, bioavailability. Statistical expertise with regard to clinical & pre clinical studies in Design; cross over, incomplete block, sample size & power. Solid knowledge & experience in computing tools such as S Plus, NONMEM, WinNonLin, SAS. Solid knowledge in global regulatory guidance documents & requirements. Solid knowledge of at least one relevant therapeutic area of drug development. Knowledge in drug absorption, distribution, metabolism, & excretion. Excellent oral & written communication skills. Excellent interpersonal skills. Excellent analytical, problem solving, & computer skills. Flexible & well organized with the initiative to take on unfamiliar tasks & work well under pressure. Must be currently residing in the U.S.Job Description: The position provides the statistical & analytical leadership to the drug development projects by exploring & defining the relationship between pharmacokinetic & pharmacodynamic data to optimize the dose & regimen selection through analysis of exposure & response. The incumbent will provide expedient & effective statistical support by using or developing advanced quantitative methodology & tools for the exploration, modeling, analysis, presentation, & interpretation of PK & PK/PD data. The incumbent will ensure compliance with appropriate global regulatory requirements & interact with domestic & foreign regulatory agencies for company’s projects. Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 108 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Cnj - Principal SAS Programmer-cPharmaceutical

Principal SAS Programmer-cPharmaceutical. Reference #: C-EE-10-349 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). Education or education/experience combination equivalent to a post graduate degree in Computer Science, Life Sciences, Statistics or Statistics related field. Four (4) years of SAS programming experience in the pharmaceutical, biotechnology, or clinical research fields having a Ph.D. or Ph.D. equivalent, 6 years of SAS programming experience in the pharmaceutical, biotechnology, or clinical research fields having a Masters degree or Masters degree equivalent, or 8 years of SAS programming experience in the pharmaceutical, biotechnology, or clinical research fields having a Bachelors degree or Bachelors degree equivalent. A minimum of 2 years of technical leadership in a statistical programming environment in a pharmaceutical, biotechnology, or clinical research fields. Excellent working knowledge of medical terminology & clinical trial methodologies. Experience in the development & implementation of statistical programming standards; knowledge of software systems development a plus. Excellent working knowledge of Base SAS, SAS/STAT, SAS Macro language & SAS SQL; SAS/GRAPH a plus. Experience with at least one UNIX Shell programming language (such as Korn Shell). Proficient in developing own code as well as modifying existing code. Excellent analytical, problem solving & organization skills with the ability to work on multiple tasks. Flexible to changing priorities, detail oriented, works well under pressure with initiative to take on unfamiliar tasks. Excellent English communication skills (verbal & written) as well as good interpersonal skills. Experience leading projects & mentoring junior programmers. Ability to travel 5 to 10 percent. Must be currently residing in the U.S.Job Description: Provide statistical programming leadership for multiple clinical/pre clinical research & development projects. Collaborate with project biostatistician in the creation, implementation, & maintenance of programming development plans for each project accounting for timelines, resources & quality deliverables for all project work assigned. Supervise the work of junior & contract programmers. Ensure that all statistical programs comply with department coding standards & utilizes available standard reporting systems, as well as utility macro programs. Provide guidance & mentoring to peer & junior programmers in statistical programming methodologies. Contribute to ongoing quality improvement efforts.Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 108 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Cnj - Manager, SAS Programming-cPharmaceutical

Manager, SAS Programming-cPharmaceutical. Reference #: C-EE-10-769 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). Degree & experience in Computer Science, Statistics, or related field. At least 8 years of pharmaceutical experience with a bachelors degree or equivalent. At least 6 years of pharmaceutical experience with a masters degree or equivalent. At least 4 years of pharmaceutical experience with a Ph.D. degree or equivalent. Minimum of 2 years of leadership role in a technical and/or statistical programming environment in a pharmaceutical or biotechnology environment. Project Management & supervisory experience in a global clinical trial environment. Experience in the development & implementation of global statistical programming standards & conventions. Excellent knowledge of clinical trial methodology & emerging global programming & data interchange standards. Demonstrated technical abilities & skills particularly in statistical software packages (e.g. SAS, S Plus). Ability in programming system development & validation. Leadership, analytical, problem solving & technical skills. Demonstrated organizational, verbal, written & interpersonal skills. Excellent ability to work on multiple projects with competing priorities. Ability to travel 5 to 10 percent. Must be currently residing in the U.S.Job Description: Plans, organizes, & manages the activities of a Statistical Programming group in support of multiple clinical projects for one therapeutic area. Ensures all statistical programming functions meet ICH/GCP quality requirements in the support of product development & life cycle maintenance. Assist in activities that apply to statistical systems development, validation & implementation including Standard Reporting Systems, SAS macro utility programs & associated tools. Develops & oversees implementation of programming standards & conventions.Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 108 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Cnj - Clean Room Supervisor (B393)

Clean Room Supervisor Clean Room Supervisor must have experience supervising in Clean Room Environment Candidates must send resume to stephanie.batchelor@expresspersonnel.com and then call Stephanie at 908 252 9520 to discuss.

Cnj - Marketing Manager

PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, medical marketing and consulting services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Headquartered near Boston, Massachusetts, PAREXEL operates in 55 locations throughout 43 countries around the world, and has over 6,315 employees. For more information about PAREXEL International visit www.PAREXEL.com. Barnett International, a division of PAREXEL, is widely recognized for its superior consulting services and its targeted education and training programs. Barnett helps clients get the most out of their research and development dollars by managing change effectively, improving organizational performance, and enhancing staff knowledge. We help pharmaceutical, biotechnology and medical device companies maximize the speed and quality of their product development efforts. With an international presence and with many staff members working from the client site for increased benefits, Barnett is able to apply a global expertise to its projects. Description: Barnett is looking for a Marketing Manager to manage all communication efforts that support the marketing planning and business development activities for all service lines of Barnett Educational Services. The responsibilities will include but are not limited to leading Barnett’s marketing efforts through the development and implementation of marketing plans for all of Barnett’s products and services, managing marketing vendors, interfacing with product development teams and developing and implementing strategies for growing Barnett’s marketing database and resources. Experience: Education: BS/BA in Marketing or business degree Minimum Work Requirements: 5+ years marketing experience, preferably in a business-to-business role Skills: Excellent oral and written communication skills; excellent project management and leadership skills; strong background marketing campaign planning and collateral development and creation; knowledge of pharmaceutical industry; excellent oral and written communication skills; strong interpersonal skills; strong MS Office skills; self motivated and ability to work independently and with a decentralized team. We have a casual, friendly, atmosphere promoting individual development and career growth. In addition, we offer a competitive salary, an excellent benefits package including tuition reimbursement, 401(k) and health insurance plans. PAREXEL is an Equal Opportunity Employer that develops strength through diversity. Please visit our web site at www.parexel.com. Please email resume to gladys.sistrunk@parexel.com

Cnj - Program Manager

PAREXEL International Corporation is a leading global bio/pharmaceutical services organization, providing a broad range of knowledge-based contract research, medical marketing and consulting services to the worldwide pharmaceutical, biotechnology and medical device industries. Committed to providing solutions that expedite time-to-market and peak-market penetration, PAREXEL has developed significant expertise across the development and commercialization continuum, from drug development and regulatory consulting to clinical pharmacology, clinical trials management, medical education and reimbursement. Headquartered near Boston, Massachusetts, PAREXEL operates in 55 locations throughout 43 countries around the world, and has over 6,315 employees. For more information about PAREXEL International visit www.PAREXEL.com. Description: The Program Manager will be responsible for the day-to-day project management of assigned client projects and multi-functional teams. The responsibilities include managing a large account and a lot of small projects, breifing clients and the internal team, keeping projects on time and within budget, setting up and maintaining monitoring and tracking systems (internal and external) and act as the key frontline member of the Client Servicing Team. Experience/Skills: - A good understanding of, and experience in, the medical communications business managing client projects (ideally for at least 3 years), and preferably with experience of working across a variety of functions -Project Management experience -Publication planning experience preferred -Ability to 'make things happen -‘Can do’ attitude -Organized, detail oriented and a self starter -Team player with good inter-personal, negotiation and organizational skills, diplomacy and tact are essential! -Excellent interpersonal, verbal and written communication skills -Project management expertise and the ability to define and refine processes -Proactive approach -Ability to relate to key client personnel and faculty in a professional and calm fashion -Proficient with Microsoft Office programs This position requires a willingness to travel to meetings etc. as needed. This position is office based and the opportunity for telecommuting will be discussed on an individual basis. We have a casual, friendly, atmosphere promoting individual development and career growth. In addition, we offer a competitive salary, an excellent benefits package including tuition reimbursement, 401(k) and health insurance plans. PAREXEL is an Equal Opportunity Employer that develops strength through diversity. Please visit our web site at www.parexel.com. please email resume to johnsore@parexel.com

Cnj - EDC Study Support Specialist

Provides ongoing support of EDC (electronic data capture) based clinical trials through the transformation of data from one database format to another, including programming in TableTrans, validation support for TableTrans diagrams, and executing diagrams on a production schedule as required by the clinical teams. 1 year assignment Minimum 3 years of pharmaceutical industry clinical development experience in clinical data management, clinical programming and/or preparation of regulaloty submissions. Good communication, documentation, planning, organizational analysis and problem solving skills. Advanced knowledge in the following disciplines: Database Support: Oracle (SQL snd PL/SQL) and Clinical or equivalent clinical database management system (Database support). Database Conversion Tools: TableTrans or equivalent SQL database conversion and export tools. Knowledge of EDC applications, on-line and off-line electronic data collection systems, and eCRF design. Degree in Life Sciences, Statistics, Mathematics, Computer Science, Medical Informatics or equivalent required For immediate consideration, please apply directly using the link below: https://www.hirebridge.com/application/appchoice.asp?jid=54674

Cnj - Environmental Scientist

Looking for candidates with Phase I experience, at least 1 yr. Please send resumes and salary requirements to nmurphy@resourceoptions.com

Cnj - Senior Clinical Data Coordinator-cPharmaceutical

Senior Clinical Data Coordinator-cPharmaceuticalReference #: C-BB-12-112 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). Bachelor’s degree in life sciences or RN preferred or equivalent work experience. Minimum of 3- 5 years clinical data management experience in a pharmaceutical or Biotech Company or CRO. Previous team leadership experience or strong management skills (someone who can move into a manager position quickly). Able to work independently & coordinate the activities of junior staff members. Thorough knowledge of applicable regulatory rules & guidelines: e.g. ICH, GCP. Strong attention to detail. Proficiency in MS Outlook, Word, Excel, PowerPoint. Knowledge of relational database structure. Familiarity with MS Internet Explorer. Basic knowledge of SQL/SAS, MS Access, MS Project is desirable.Job Description: Provide leadership & expertise for all data management activities for multiple projects. Work independently & coordinate the activities of junior staff members. Ensure timely & accurate completion of all data management activities. Assume primary/lead responsibility for the execution of assigned projects. Demonstrate strong data management knowledge & skills. Provide leadership for all data management activities to ensure database accuracy across projects assigned. Provide project status reports to the Project Team as requested. Participate in the development of new SOPs & revision of current SOPs. Engage in data management related systems validation. Assist with special projects & other duties as required.Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 136 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Cnj - Principal Biostatistician/Manager Biostatistics-cPharmaceutical

Principal Biostatistician/Manager Biostatistics-cPharmaceuticalReference #: C-EE-11-662 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). Education or education/experience combination equivalent to a post graduate degree in statistics or statistics related field. At least 2 years of pharmaceutical experience with a Ph.D. or Ph.D. equivalent. At least 4 years of pharmaceutical experience with a Masters degree or Masters degree equivalent. Statistical experience with regard to clinical studies in at least one topic of design; cross over, multiplicity, interim analyses, non inferiority, sample size and/or power. Statistical experience with regard to clinical studies in at least one topic of analysis; treatment by center interaction, multi center, missing value imputation, covariate, and/or subpopulations. Statistical experience with regard to clinical studies in at least one topic of for each methodology; analysis of variance & mixed linear models, survival analysis, categorical data analysis, reliability, multivariate analysis, robust estimation, nonparametric techniques, and/or group sequential analyses. Knowledge of global regulatory guidance documents & requirements. Working knowledge of SAS. Excellent oral & written communication skills. Excellent interpersonal skills. Excellent analytical, problem solving, & computer skills. Flexible & well organized with the initiative to take on unfamiliar tasks & work well under pressure. Must be currently residing in the U.S.Job Description: As the project statistician for assigned clinical programs, the position represents BDMP on project teams, plans all aspects of data analysis for assigned projects, has responsibility for the preparation & maintenance of the Analysis Plan (AP), & ensures the quality controlled production of all tables, listings & graphs for the clinical document while adhering to the pre specified analyses & timelines. The position may serve on departmental teams & make recommendations for departmental standards.Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 136 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Cnj - Biostatistics Manager II-cPharmaceutical

Biostatistics Manager II-cPharmaceuticalReference #: C-EE-11-275 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). Education or education/experience combination equivalent to a post graduate degree in statistics or statistics related field. At least 5 years of pharmaceutical experience with Ph.D. or Ph.D. equivalent or 7 years of pharmaceutical experience with a Masters degree or Masters degree equivalent. Statistical expertise with regard to clinical studies in Design including cross over, multiplicity, interim analyses, non inferiority, sample size & power. Statistical expertise with regard to clinical studies in Analysis including treatment by center interaction, multi center, missing value imputation, covariate, & subpopulations. Statistical expertise with regard to clinical studies in Methodology including analysis of variance & mixed linear models, survival analysis, categorical data analysis, reliability, multivariate analysis, robust estimation, nonparametric techniques, & group sequential analyses. Solid knowledge in global regulatory guidance documents & requirements. Working knowledge of SAS. Excellent oral & written communication skills. Excellent interpersonal skills. Excellent analytical, problem solving, & computer skills. Flexible & well organized with the initiative to take on unfamiliar tasks & work well under pressure. Must be currently residing in the U.S. Job Description: As the project statistician for assigned clinical programs, the position represents the group on project teams advising team members in drug development strategies, plans all aspects of data analysis for assigned projects, has responsibility for the preparation & maintenance of the Analysis Plan (AP), & ensures the quality controlled production of all tables, listings & graphs for the clinical document while adhering to the pre specified analyses & timelines. This position interacts with domestic & foreign regulatory agencies for company’s projects. The position may serve on company and/or departmental teams & make recommendations for departmental standards. Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 136 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Cnj - Senior Programmer-cPharmaceutical

Senior Programmer-cPharmaceuticalReference #: C-EE-10-320 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). Education or education/experience combination equivalent to a post graduate degree in Computer Science, Life Sciences, Statistics or Statistics related field. 2 years of pharmaceutical clinical research experience with a masters degree or masters degree equivalent, or 4 years of pharmaceutical clinical experience with a bachelors degree or bachelors degree equivalent. Working knowledge of medical terminology, clinical trial methodologies, & software systems development. Working knowledge of at least one scientific programming language & at least one statistical software package (such as SAS, S Plus). Working knowledge of at least one database system. Excellent analytical, problem solving, & computer skills. Flexible, well organized, excellent verbal & written communication skills, & interpersonal skills. Works well under pressure, with initiative to take on unfamiliar tasks. Must be currently residing in the U.S.Job Description: Provides statistical programming support for multiple clinical/preclinical research & development projects. Collaborates with project biostatistician in the creation, implementation, & maintenance of execution plan accounting for timeline, resource & quality of the projects. Ensures that all statistical programs comply with the programming coding standards & utilize available standard reporting systems, as well as macro utility programs.Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 136 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Cnj - Principal Statistical Development Programmer-cPharmaceutical

Principal Statistical Development Programmer-cPharmaceuticalReference #: C-EE-10-417 (include reference number when responding) Job Requirements: All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). Degree & experience in Computer Science, Statistics, or related field. At least 8 years of pharmaceutical experience with a Bachelors degree or equivalent. At least 6 years of pharmaceutical experience with a Masters degree or equivalent. At least 4 years of pharmaceutical experience with a Ph.D. degree or equivalent. Minimum of 2 years of technical leadership role in a statistical programming environment in a pharmaceutical or biotechnology environment. Experience in the development & implementation of global statistical programming standards & conventions. Excellent knowledge of clinical trial methodology & emerging global programming & data interchange standards. Ability in development & validation of programming systems. Demonstrated technical abilities & skills of at least one scientific programming language & at least one statistical software package (such as SAS, S Plus, SQL). Working knowledge of at least one database system. Analytical, problem solving, & computer skills. Flexible, demonstrated organizational, verbal, written & interpersonal skills. Excellent ability to work on multiple projects with competing priorities. Ability to travel 5 to 10 percent. Must be currently residing in the U.S.Job Description: As a technical lead, this position develops cost efficient, innovative, hardware independent, globally oriented, flexible, expandable, user friendly computer software systems for statistical applications. Expands & broadens the scope of scientific programming support with efficiency, quality, & regulation compliance in the area of pharmaceutical research.Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 136 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Cnj - Director, Hematology/Oncology-cPharmaceutical

** position can be filled at Associate Director or Executive Director level ** Will consider home-based arrangement in any location in the USA for Exec Dir level Reference #: C-TL-0-4-795 (include reference number when responding) Job Requirements: A medical degree from an accredited & internationally recognized medical school with a curriculum relevant to general medical education & training, Board Certification in Hematology/Oncology, along with a medical license to practice in the US is required. No clinical research experience required. Ability to establish & meet priorities, deadlines, & objectives. Skills in providing consultation & advice on multiple assignments required, as well as initiative & flexibility. ** Position will be filled at a level appropriate to one’s background – from an Associate Director level up to Executive Director level. MUST have pharmaceutical industry experience (or will also consider CRO experience).All our positions require prior work experience at a pharmaceutical, biotech/pharma, or CRO (Clinical Research Organization). Job Description: The Medical Advisor participates in all aspects of Medical & Scientific Services' involvement on assigned trials. Provides medical support to investigative sites & project staff for protocol-related issues including protocol clarifications, inclusion/exclusion determinations, & issues of patient safety and/or eligibility. Performs review & clarification of trial-related Adverse Events (AEs). Performs medical case review of Serious Adverse Events (SAEs), including review of case documentation & patient narrative. Provides medical support for the Analysis of Similar Events (AOSE). Performs medical review of Adverse Event coding. Performs medical review of the protocol, Investigative Drug Brochure (IDB), and/or Case Report Forms (CRFs). Performs review of the Clinical Study Report (CSR) & patient narratives. Available 24 hours per day, 7 days per week to respond to urgent protocol-related issues at the investigative sites. Attends & presents at Investigator Meetings. Provides therapeutic area/indication training for the project clinical team. Attends meetings, as needed or requested. Serves as Scientific Advisor & provides guidance to Project Managers on the medical & scientific aspects of assigned projects.Please Note:We represent only professionals who have prior work experience in the pharmaceutical / biotech industry. All our positions are listed at www.landmarksearch.com. All our positions are permanent, full-time, office-based positions. Most positions have relocation assistance.Please email resume as a Word attachment to melissa@landmarksearch.com for confidential consideration for this and any of our other 124 positions in the pharma/biotech industry.We give you additional details about the company and the position after you submit your resume to us and after we review your career goals with you. To protect your confidentiality, your resume is NOT submitted to any of our client companies without your prior authorization.

Cnj - BioBook Consultant I

We are currently recruiting for: Talented individuals to help expand our U.S. based operations and grow our portfolio of products and new customers! IDBS’ domain expertise in biology and chemistry data management delivers value to the life science industry worldwide. We work with many of the major pharmaceutical and biotech companies to enable discovery organizations to capture, analyze, store, and share research data. By integrating biological and chemical data into a scalable and extensible environment, our software protects the principle assets of discovery organizations. We are currently recruiting for consultants to help design and deliver enterprise solutions for our regional BioBook customers. BioBook provides complete data management for companies involved in late stage discovery and preclinical research. The BioBook Consultant I will be responsible for assisting BioBook customers with general consulting, template building, end-user training, and application testing. Successful candidates will have a background in life science, a strong interest in computer-related technologies for the pharmaceutical sector, and enjoy working with customers to maximize the value of our products. Responsibilities: •General consultancy and template building for our broad customer base. •Provide on-site installation and configuration support. •Conduct requirements analysis for customer templates. •Deliver standard IDBS product-training courses. •Assist with GMP, GLP, and compliance related issues as they relate to our product and our customers. •Offer sales support through application assistance and template building. •Obtain customer feedback as a means to drive new product development. •Identify new sales opportunities in the existing customer base. •Participate in project management for smaller consultancy assignments. •Perform application testing and provide help desk support. •Reports to the Regional Manager of Professional Services. Requirements: •Previous experience working within or supporting research in pharmacology, drug metabolism, pharmacokinetics, toxicology, or safety science. •Experience working with statistical analysis methods and their applications. •Familiar with GMP, GLC, and general compliance related issues. •Background working in pharmaceutical or biotech companies. •Demonstrate ability to formulate targeted questions in working with customers, •Must be able to respond to customer questions and feedback in a professional, timely, and confident manner. •Excellent verbal communication skills both with colleagues and customers. •Strong technical writing skills and the ability to document requirements and workflow analysis. •Possess a strong work-ethic and professional demeanor. •Excellent presentation, communication, and interpersonal skills. •Flexible and adaptable to changing customer needs and work environments. •Must exhibit a confidence and enthusiasm for working with new customers and new challenges. •Possess strong common-sense for understanding and responding to customer needs. •Work well independently and in team environments. •Self-motivated and focused on high-quality performance. •Programming skills, including .NET, and JAVA. •Technical experience with ActivityBase, other bioinformatics or cheminformatics data management systems, or other LIMS systems, as well as experience with GraphPad Prism, Sigma Plot, WinoNonLin, SAS, R, JMP and other major statistical packages. •General IT skills and database experience. •Graduate level work in Biology or Chemistry. •1-3 years post-graduate experience. •Informatics professionals supporting the life science and pharmaceutical sector are also encouraged to apply. •Ideal candidates enjoy working with computers and database solutions and are looking for professional growth opportunities. •Regional travel varies over periods of time, but on average amounts to approximately 25-50%. Visit our website to learn more about IDBS and our BioBook offering! www.idbs.com TO APPLY FOR THIS POSITION please email your resume & cover letter to jbaluyot@thinkhr.com.

Cnj - ActivityBase Consultant I

We are currently recruiting for: Talented individuals to help expand our U.S. based operations and grow our portfolio of products and new customers! IDBS’ domain expertise in biology and chemistry data management delivers value to the life science industry worldwide. We work with many of the major pharmaceutical and biotech companies to enable discovery organizations to capture, analyze, store, and share research data. By integrating biological and chemical data into a scalable and extensible environment, our software protects the principle assets of discovery organizations. We are currently recruiting for positions to help design and deliver enterprise solutions for our regional ActivityBase customers. The ActivityBase suite remains a leader in high volume screening to low throughput data management providing a secure, consistent and accessible environment for companies managing research data. The ActivityBase Consultant I will be responsible for assisting ActivityBase customers with general consulting, template building, end-user training, and application testing. Successful candidates will have a background in life science, a strong interest in computer-related technologies for the pharmaceutical sector, and enjoy working with customers to maximize the value of our products. Responsibilities: •General consultancy and template building for our broad customer base. •Provide on-site installation and configuration support. •Conduct requirements analysis for customer templates. •Deliver standard IDBS product-training courses. •Offer sales support through application assistance and template building. •Obtain customer feedback as a means to drive new product development. •Identify new sales opportunities in the existing customer base. •Participate in project management for smaller consultancy assignments. •Perform application testing and provide help desk support. •Reports to Regional Manager of Professional Services. Qualifications: •Experience working in pharmaceutical or biotech companies, as well as demonstrated laboratory work experience. •Demonstrate experience working within or supporting high throughput screening and knowledge in plate-based screening. •Technical experience with ActivityBase, other bioinformatics or cheminformatics data management systems, or other LIMS systems. •Experience working with statistical analysis methods and their applications. •Strong technical writing skills and the ability to document requirements and workflow analysis. •Ability to formulate targeted questions in working with customers. •Must be able to respond to customer questions and feedback in a professional, timely and confident manner. •Excellent verbal communication skills both with colleagues and customers. •Possess a strong work-ethic and professional demeanor. •Excellent presentation, communication, and interpersonal skills. •Flexible and adaptable to changing customer needs and work environments. •ActivityBase Consultant I candidates must exhibit a confidence and enthusiasm for working with new customers and new challenges. •Possess strong common-sense for understanding and responding to customer needs. •Work well independently and in team environments. •Self-motivated and focused on high-quality performance. •Programming skills, including PL/SQL. •General IT skills and database experience. •Experience using Oracle database systems. •Expert level experience using Microsoft Excel. •Ideal candidates enjoy working with computers and database solutions and are looking for professional growth opportunities. •Graduate level work in Biology or Chemistry. •1-3 years post-graduate experience. •Regional travel varies over periods of time, but on average amounts to approximately 25-50%. Visit our website to learn more about IDBS and the ActivityBase Suite www.idbs.com TO APPLY FOR THIS POSITION please email your resume & cover letter to jbaluyot@thinkhr.com.