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    1. Regulatory CMC Associate Manager - NJ - 6 months (97610 - KD)

      Assist and support regulatory CMC managers in the following activities: Defining global CMC regulatory strategy and decisions for development projects or marketed products to achieve optimal submission/approval results and ensure regulatory compliance. Communicating CMC ...

    2. 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 ...

    3. Senior Executive Director, Ophthalmology Programs

      Senior Executive Director, Ophthalmology Programs Job Summary: Scientific Search client has an immediate need for a Sr. Executive Director, Ophthalmology Programs. Our client is an accomplished Clinical Leader with expertise in one of our key therapeutic areas; ...

    4. Medical Writer

        Medical Writer Responsibilities: · Writing, editing, reviewing and formatting documents that conform to domestic and/or international regulatory submissions and internal document standards, while meeting project timelines. · Carries out core-level responsibilities with ...

    5. Alliance Manager -- Oncology

       My client seeks an Alliance Manager to provide scientific and technical promotion for their services and form strategic research and clinical collaborations.  The Medical Science Liaison will bring new sites on board and work with current sites to maximize enrollment in ...

    6. How to Become Clinical SAS Programmer  :  AWARENESS SESSION

      Subject : How to Become Clinical SAS Programmer  - AWARENESS SESSION   Dear Candidate,   LEARNING's FOR JOB (HOME-BASED) We thank you for your application and interest in our Online Training and Internship program. Below are the learning you will gain thru this Online ...

    7. How to Become Clinical Research Associate: AWARENESS SESSION

      Subject : How to Become Clinical Research Associate  - AWARENESS SESSION Dear Candidate, LEARNING's FOR JOB (HOME-BASED)   We thank you for your application and interest in our Online Training and Internship program. Below are the learning you will gain thru this Online ...

    8. 97511 – Manager, Clinical Trials

        Job Description: Responsible for implementation and management of all aspects of clinical trial activities. Contributes to the long term development goals of the assigned project(s) in collaboration with senior management. Reporting Relationship: Senior Manager, ...

    9. 97513 – Clinical Trials Coordinator

        Job Description: The Clinical Trial Coordinator is primarily responsible for providing support to the Study Team(s) to assist with the execution and maintenance of clinical studies.   Responsibilities include: •  Assisting with tracking study progress and maintaining ...

    10. Clinical Research Associate -  In-House - 97512

          Senior Clinical Research Associate / CNS Therapeutic area Working onsite in Princeton, NJ Position requires a minimum of a Bachelor’s degree, preferably in a health/medical related field or life sciences - Minimum of 4 years of clinical trial experience in the ...

    11. Clinical Trial Coordinator /  Clinical Research Coordinator

      Title:  Clinical Trial Coordinator  Location:  Princeton, NJ  (work onsite)   Responsibilities include: •  Assisting with tracking study progress and maintaining study status updates (e.g., IRB approvals, regulatory document collection, patient enrollment, monitoring ...

    12. Medical Writer

        Medical Writer Responsibilities: · Writing, editing, reviewing and formatting documents that conform to domestic and/or international regulatory submissions and internal document standards, while meeting project timelines. · Carries out core-level responsibilities with ...

    13. Medical Writer

        Medical Writer Responsibilities: ·         Writing, editing, reviewing and formatting documents that conform to domestic and/or international regulatory submissions and internal document standards, while meeting project timelines. ·         Carries out core-level ...

    14. 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 ...

    15. 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 ...

    16. Senior Executive Director, Ophthalmology Programs

      Senior Executive Director, Ophthalmology Programs Job Summary: Scientific Search client has an immediate need for a Sr. Executive Director, Ophthalmology Programs. Our client is an accomplished Clinical Leader with expertise in one of our key therapeutic areas; ...

    17. Senior Executive Director, Ophthalmology Programs

      Senior Executive Director, Ophthalmology Programs Job Summary: Scientific Search client has an immediate need for a Sr. Executive Director, Ophthalmology Programs. Our client is an accomplished Clinical Leader with expertise in one of our key therapeutic areas; ...

    18. Clinical Trial Document Auditor (GCP)

      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 Quality Auditor of their ...