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    Clinical Scientist III - Cambridge, United States - Randstad Life Sciences US

    Default job background
    Pharmaceutical / Bio-tech
    Description

    This position is anticipated to open within the next couple of months**

    We are seeking a PhD, PharmD, or MD Clinical Scientist for our Global Pharmaceutical Client in Cambridge, MA. Very attractive pay rate

    This role will support a director in the medical scientific contribution to the clinical study (protocol development, validation of study data, review of study plan, managing study committees).

    Details:

    • 1-year renewable contract
    • Hybrid schedule (minimum of 2 days per week onsite at Waters St location in Cambridge)
    • This person will join a team supporting global late-phase clinical programs.

    Must haves:

    • Must have experience in late-stage clinical trials, medical monitoring, and data reviews
    • Previous experience with protocol development
    • Previous experience in neurology, neuroscience preferred
    • Previous senior clinical scientist experience

    The primary purpose of the Clinical Scientist's position is to assist/support the Clinical Research Director in the medical/scientific contribution for the clinical studies e.g: supporting operational activities about the abbreviated protocol/protocol/amended protocol development (such as contribution to the writing of protocol and/or amendments, informed consent, committees charters development, and other study ancillary documents), support in the validation and clinical case review of study data, review of study plans and draft study reports/publications for accuracy, a search of medical/scientific information for study teams, literature review and analysis, assists in the preparation of the responses for investigators, study teams, ethics committees or regulatory authorities, help manage study committees.


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