Overview
In this Medical Director role, you provide medical, scientific, and strategic leadership for planning, executing, and reporting clinical trials. You act as the internal medical expert, supporting study reports, regulatory documents, and interpretation of results. You will contribute to new clinical projects, including study design, protocol creation, and project plans, while coordinating across departments. This hybrid, flexible-role fits a mission-driven CRO focused on accelerating therapeutic development. You will shape trial design and safety oversight to advance meaningful clinical outcomes.
Pay / Benefits
- flexible work environment
- competitive compensation and benefits package
- competitive PTO packages
- structured career paths with opportunities for professional growth
- 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 documents, and manuscripts
- Manage safety issues and evaluate trials with colleagues
- Participate in business development through proposals and sponsor meetings
- Coordinate with other departments across feasibility, design, medical information, and editing of medical documents
- Lead adherence to research protocols and policies
Key requirements
- M.D. degree or equivalent
- Board certification and current medical licensure preferred
- Prior clinical trial research experience preferred
- Previous experience in pharmaceutical-related clinical research preferred
- leadership
- cross-functional collaboration
- strong communication
- clinical trial leadership
- protocol design
- study design
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