Executive Medical Director, Clinical Development - San Diego, United States - Rbw Consulting

    Rbw Consulting
    Rbw Consulting San Diego, United States

    2 weeks ago

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    Description
    Senior/Executive Medical Director, Clinical DevelopmentRBW is partnered with a well-funded US based biotech with a startup environment. This biotech focuses on Endocrine and Metabolic Disorders and is looking to potentially expand into other areas.

    Following positive data in their Phase 2 NASH trial, this biotech is looking to add multiple headcount to their team including hiring their first permanent MD.Job SummaryOur client is looking to hire an experienced science-oriented Senior Medical Director to Vice President with Clinical Development experience.

    This role will report directly to the C-Suite and will be responsible for the development of clinical research strategies and direction of Phase 1-3 clinical studies in Endocrine and Metabolic disorders and Rare Diseases.

    This role is a great opportunity to be one of the first Clinical Development team members and have the opportunity to grow with them as they continue to move their products forward.

    Job ResponsibilitiesExpertise in medical and scientific fields is crucial for the success of clinical trials and development of effective treatments.

    Provide clinical and scientific input for study design, protocol concepts, statistical analysis plans, and reporting to ensure valuable clinical endpoint insight for future decision-making.

    Sound scientific and clinical judgement is essential to interpret clinical trial data accurately.

    Collaboration with external opinion leaders, Principal Investigators, and clinical operations personnel is necessary for successful implementation of appropriately designed studies.

    Familiarity with clinical research and trial design concepts, including biostatistics.
    Developing scientific relationships with external opinion leaders and presenting at advisory boards, scientific meetings, and external committee meetings.

    Serve as the Medical Monitor for clinical trials to ensure safety monitoring and act as the medical expert for clinical studies.

    Participate in the preparation of abstracts, manuscripts, and presentations for external meetings and author clinical sections of regulatory documents (IB, IND sections).QualificationsMD (no specific subspecialty training required).2-10 years of industry clinical development experience.

    Experience in Endocrine and Metabolic Disease drug development is a plus.#J-18808-Ljbffr