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    1. Director, Medical Science

      Director, Medical Science, Summit NJ area MUST HAVE MD-PLEASE DO NOT APPLY IF NOT AN MD SUMMARY The Director of Medical Science (MS) is responsible for providing input into the Global Project Teams in planning, designing, developing, executing and interpreting clinical ...

    2. Medical Writer - Biopharma

      Are you seeking an opportunity with a rapidly growing biopharmaceutical company developed life-changing therapies in the greater Princeton area? A pharmaceutical sponsor of drugs impacting lives with rare and orphan diseases is seeking a strong Medical Writer to help with ...

    3. Director, Medical Science

      Director, Medical Science, Summit NJ area MUST HAVE MD-PLEASE DO NOT APPLY IF NOT AN MD SUMMARY The Director of Medical Science (MS) is responsible for providing input into the Global Project Teams in planning, designing, developing, executing and interpreting clinical ...

    4. Medical Writer - Biopharma

      Are you seeking an opportunity with a rapidly growing biopharmaceutical company developed life-changing therapies in the greater Princeton area? A pharmaceutical sponsor of drugs impacting lives with rare and orphan diseases is seeking a strong Medical Writer to help with ...

    5. Medical Writer

        Responsibilities- Medical Writer Research and write training materials delivered to pharmaceutical, medical device, and/or biotech sales representatives. The end product includes but is not limited to print modules, e-learning programs, and workshop materials Consult ...

    6. Project Manager I

        PROJECT MANAGER Serving as the primary point of contact for external client contacts as well as an internal multi-functional team Managing project budgets, timelines, resources, and deliverables (including, but not limited to, e-learning, mobile, virtual ...

    7. Pharmacovigilance Specialist

      Vivos Professional Services is presently seeking candidates for a Pharmacovigilance Specialist position in Princeton, NJ.   This role will be responsible for the processing of adverse event information from all sources including clinical trials, post-marketing and published ...

    8. Clinical Project Manager

      Our Client is looking for a dynamic Clinical Project Manager to join their team.  The Clinical Project Manager (CPM) is responsible and accountable for the monitoring and management of scope, cost, schedule and quality of assigned clinical studies, projects and corporate ...

    9. Validation Engineer - Mid Atlantic Region

      Here at ProPharma Group, we work with clients in the pharmaceutical, biotechnology and medical device industries to provide the best solutions for their unique challenges and concerns. We build successful long-term relationships with clients by providing leading industry ...

    10. Director, Medical Science

      Director, Medical Science, Summit NJ area MUST HAVE MD-PLEASE DO NOT APPLY IF NOT AN MD SUMMARY The Director of Medical Science (MS) is responsible for providing input into the Global Project Teams in planning, designing, developing, executing and interpreting clinical ...

    11. Epidemiologist

        Under the direction of the Epidemiology team’s leadership, the Epidemiologist will work with the members of the Clinical Safety & Pharmacovigilance Product Teams to assist with various components of Epidemiology deliverables.   Responsibilities   Conduct systematic ...