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    Medical Director/Senior Medical Director - Los Angeles, United States - GQR

    GQR background
    Description
    The Director/Senior Medical Director, reporting to the Chief Medical Officer, plays a pivotal role in steering clinical development initiatives.

    With a focus on ensuring adherence to GCP, SOPs, and regulatory standards, this role orchestrates the planning and execution of clinical studies, driving programs through the research process efficiently.


    Key Responsibilities:


    Design, oversee, and execute clinical deliverables to support defined program objectives, including document development, contribution to key documents, and providing medical and scientific input throughout study lifecycle.

    Review, analyze, interpret, and present clinical data internally and externally, representing clinical studies or programs on relevant teams or subteams.

    Develop and optimize KOL and investigator communication strategies, organizing advisory board and investigator meetings as needed.


    Qualifications, Education & Experience:
    MD or non-US equivalent.
    10+ years of clinical trial experience encompassing early and late-phase development, with at least 7 years in the industry.

    Consideration may be given to candidates with exceptional experience in other therapeutic areas, particularly if they demonstrate potential for application in oncology.

    Expertise in radiopharmaceuticals is a plus.
    Profound understanding of clinical development phases, including familiarity with drug approval processes in the US and internationally.
    Experience in all aspects of protocol conduct, from writing to execution, analysis, and reporting.
    Strong knowledge of FDA regulations, Good Clinical Practices, and clinical trials guidelines.

    *By applying for this position, you agree to receive marketing communication from GQR and agree to our GQR Privacy Policy & GQR Terms of Use. You may unsubscribe at any given time.

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