Study Director

4 weeks ago


Lexington, United States Medix™ Full time

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 Master’s Degree; 5+ years with a Bachelor’s Degree, preferably in pharmaceuticals or contract laboratories.
  • Ideally surgical experience with animals


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