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    Study Director - Lexington, United States - Medix

    Medix
    Medix Lexington, United States

    3 weeks ago

    Default job background
    Description

    Key Responsibilities:

    • Provide client insights on pre-clinical testing regulations.
    • Act as an autonomous Study Director adhering to GLPs.
    • Interpret local regulations and expand service offerings accordingly.
    • Supervise study processes from inception to reporting.
    • Coordinate study execution independently.
    • Utilize diverse subcontracted services and scientific disciplines.
    • Host client meetings and virtual conferences independently.
    • Contribute to projects, mentoring junior staff as needed.
    • Provide client and technical team support.
    • Assist in budgeting and resource allocation.
    • Attend scientific events and drive exploration of new service areas.

    Additional Requirements:

    • Excellent communication and client engagement skills.
    • Analytical and problem-solving abilities.
    • Proficiency in computer applications and GLP regulations.
    • Strong organizational skills and deadline adherence.
    • Leadership and team management skills.

    Qualifications:

    • Education: Advanced degree in a relevant field or equivalent experience.
    • Experience: 1-2 years with a DVM or PhD; 2-5 years with a Masters Degree; 5+ years with a Bachelors Degree, preferably in pharmaceuticals or contract laboratories.
    • Ideally surgical experience with animals
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