Overview
In this role you will provide medical leadership for clinical trials and act as the internal medical expert, guiding study design, safety management, and interpretation of results. You will contribute to study reports, regulatory documents, and manuscripts while supporting new clinical projects and sponsor discussions. You will collaborate with cross-functional teams to ensure compliant, high-quality trial execution. This position blends medical expertise with strategic planning to advance therapeutic development at Medpace.
Pay / Benefits
- Flexible work environment
- Competitive compensation and benefits package
- Competitive PTO packages
- Structured career paths with growth opportunities
- Company-sponsored employee appreciation events
- Employee health and wellness initiatives
Responsibilities
- Provide medical management and expertise for clinical trials
- Contribute medical input to study reports, regulatory docs, and manuscripts
- Manage safety issues and collaborate with the team on evaluation of trials
- Engage in business development through proposals and sponsor meetings as needed
- Coordinate with other departments across feasibility, design, medical information, and document review/editing
- Follow protocol requirements and lead others in adherence to policies
Key requirements
- MD degree or equivalent
- Board certification and licensure preferred
- Prior clinical trial research experience preferred
- Experience in pharmaceutical-related clinical research preferred
- leadership in medical context
- cross-functional collaboration
- clear communication with stakeholders
- clinical trial oversight
- study design and protocol development
- medical monitoring and safety evaluation
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