Hepatology Clinical Trials Director (Hybrid)

Medpace, Inc.

Warszawa

Hybrid

PLN 603,000 - 753,000

Full time

14 days+

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Job summary

Medpace, Inc. seeks a Hepatologist to join our team in London in a Medical Monitor role overseeing medical leadership for clinical trials. This position includes medical management, review of study results, and input into protocol design, with hybrid work-from-home flexibility.

Applicants should hold an MD, with board certification and current medical licensure preferred, and have prior clinical trial experience or pharmaceutical research background.

Qualifications

  • MD degree or equivalent; board certification and licensure preferred.
  • Prior clinical trial research experience preferred.
  • Previous experience in pharmaceutical-related clinical research is preferred.

Responsibilities

  • Provide medical management and expertise for clinical trials;
  • Contribute medical expertise to study reports, regulatory documents, and manuscripts;
  • Manage safety issues in clinical trials and work closely with associates in evaluation and assessment of the trials;
  • Participate in new business development through involvement in proposal and sponsor meetings as requested;
  • Coordinate with other departments in all phases of the studies and trials including feasibility assessments, design processes, educational efforts, management of medical information, and reviewing and editing of medical documents;
  • Follow specific research related protocol and lead others in strict adherence to the policies.

Education

MD degree or equivalent
Board certification preferred
Current medical licensure preferred

Job description

Medpace, Inc. seeks a Hepatologist to join our team in London in a Medical Monitor role overseeing medical leadership for clinical trials. This position includes medical management, review of study results, and input into protocol design, with hybrid work-from-home flexibility.

Applicants should hold an MD, with board certification and current medical licensure preferred, and have prior clinical trial experience or pharmaceutical research background.

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