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Publicly traded Boston based pharmaceutical company is expanding and looking for: experienced Associate Director of Clinical Trial Disclosure and Transparency to lead, define, execute, and efficiently manage clinical trial disclosure and transparency activities. This newly created position will report to the Head of Medical Writing and will be a key player in evaluating, developing, and implementing efficient, quality compliant processes and systems to ensure overall effectiveness. In....

- Cambridge, MA

Summary of Key ResponsibilitiesProduce high quality and on-time writing deliverables.Plan, write, edit, and format key documents with minimal supervision, including clinical protocols, investigator brochures, clinical study reports, integrated safety and efficacy summaries and related documents. Other documents may include informed consent forms, health authority briefing books, and scientific publications.Facilitate efficient review and finalization process for documents produced internally....


Global Pharmaceutical company is hiring a Director, Scientific Communications- VERY COMPETITIVE base salary, bonus, stock and other Long Term Incentives Succesfull Pharma with marketed products and pipeline of product candidates for chronic diseases that include schizophrenia, depression, addiction and multiple sclerosis. Headquartered in Dublin, Ireland, Company has an R&D center in Waltham, Massachusetts; a research and manufacturing facility in Athlone, Ireland; and a manufacturing....

- Bridgewater, NJ

Global Pharmaceutical company in Bridgewater, NJ is looking to a hire a Manager, Medical Education one year, w-2 contract, full benefits and competitive salaryob Summary: The Medical Education Associate Manager is responsible for the development and management of a portfolio of non-accredited medical education programs and speaker management. Principle Responsibilities: (essential job duties and responsibilities) - Develop and execute medical education program plan o Initiate and lead....


Clinical Systems Manager opportunity for a teaching hospital system in upstate New York. Responsibilities: Manage a team of systems analysts who support several hospital IT systems, including OR scheduling and peri-operative documentation, anesthesia documentation, Telehealth and other applications. The manager provides technical and operational oversight and direction to staff and ensures organizational activities and structures are developed to meet established needs. Requirements:BS in IT,....


My client is expanding and looking to hire a Manager for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharma and biotech partners and facilitate work with biotech Directors and VPs, academic PIs, and others.Understand the research and drug development needs of existing partners and ensure exceptional service.Develop and expand research and clinical collaborations with new partners. The ideal candidate will....


My client is expanding and looking to hire a Manager for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharma and biotech partners and facilitate work with biotech Directors and VPs, academic PIs, and others.Understand the research and drug development needs of existing partners and ensure exceptional service.Develop and expand research and clinical collaborations with new partners. The ideal candidate will....


My client is expanding and looking to hire a Manager for their Medical Affairs group. The ideal candidate will take on the following responsibilities:Direct collaborations with academic, pharma and biotech partners and facilitate work with biotech Directors and VPs, academic PIs, and others.Understand the research and drug development needs of existing partners and ensure exceptional service.Develop and expand research and clinical collaborations with new partners. The ideal candidate will....


This dynamic department is looking for an HEOR professional (AD Level) he/she will be responsible and accountable for project execution and strategic support for Company’ products throughout their lifecycle. He/she will help to develop and implement US economics and outcomes strategy for one or multiple therapeutic area(s). This is a strategic as well as a technical position with project-specific responsibilities. This individual will ensure that rigorous health economics and outcomes research


Director, Medical Information for this leading pharmaceutical company in New England S Headquarters in Waltham, MA Looking for Senior Engineer for drug product unit operations- leadership scale-up and optimization in development from R&D to cGMP Phase 3 manufacture to process validation. Experience with continuous manufacturing, scale-up and PAT implementation is strongly desired. The individual is expected to integrate QbD principles, guide experimental design with a focus on process....


Leading Pharmaceutical Company with marketed products and strong Neurology Pipeline is looking for a Director, Medical Information for their growing US Headquarters in Waltham, MA Competitive Base, Bonus, Long Term Incentives and Relocation The Director, Medical Information (MI) will be responsible for leading the MI function within the Medical Affairs. The Director, Medical Information will be responsible for managing the member of the MI function who are providing and supporting the....


Strong Player in the Pharmaceutical Industry is looking to hire a Medical Director for their new Phase one Unit (24 bed) Looking for a true Medical Director (not just a PI) who can interact and engage other Key Opinion Leaders in the Medical Community This role include VERY competitive base salary, long term incentive and full relocation (will make it stress free- pack up, moving and temp housing, real estate assistance and more) The primary responsibilities of this position include medical....

- Decatur, IL

Global Specialty Pharmaceutical company is expanding in their Decatur, IL location Need Process Engineer III will relocate competitive and comprehensive salary and benefits hile a member of the Technical Services organization, the Process Engineer will be located on the manufacturing site located in Decatur, IL. The Process Engineer will be responsible to provide the plant operations unit technical process expertise for a variety of pharmaceutical configurations produced on-site. The scope of....


Global Pharmaceutical Leader is looking for consultant (all levels) Clinical Managers for their growing Clinical Development team Accountable for leading the operational study team, which is responsible for the execution and delivery of quality studies, including in-process quality control activities (e.g. quality checks and balances to ensure inspection readiness, enrollment, metrics, milestones, timelines and budget). This position requires advanced knowledge of the functional disciplines....


Top Tier Pharmaceutical company (with focus in RESPIRATORY, CNS, Diabetes, Cardio, GI and more) in Madison, NJ is looking for three Clinical Trials Manager Consultants for Clinical Trials Group This is a one year contract and can continue for up to 4 years (1099 or w-2)SummaryParticipate in all aspects of clinical development and study management under the direction of the Director, or designee, which includes providing scientific, and/or logistical support to planned and ongoing trials CTM –....

- Swifwater, PA

Global Pharmaceutical and Vaccine company is expanding the Marketing division: Objective: To maximize company dose and dollar sales volume in a manner consistent with profit goals. Expectations: ·Achieve forecast as planned. ·Develop realistic and achievable forecast in concert with Marketing and Sales Management. ·Use information systems and reports to monitor and direct the progress of sales and profits toward monthly, trimester and annual sales objectives. PRODUCT LINE MANAGEMENT Objective:

- Waltham, MA

Incredibly successful publicly traded Biotech in Waltham , Massachusetts is expanding due to their clinical trial success. Looking for a Strong Clinical Trials Manager or Senior Clinical Trials Manager to help lead their Phase 2 and 3 trials in anti-cancer partner drugs. This company has three wholly owned therapies- in late stages, with a fourth starting in phase I. This CTM is focused on the anti- cancer phase III trials. If you are an experienced Clinical Trials Manager with oncology....

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