Lead medical oversight for clinical trials across one or more therapeutic areas, serving as the internal medical expert for study design, safety review, and interpretation of trial results. This role supports protocol development, clinical study reports, regulatory documents, and manuscript preparation while partnering with cross-functional teams throughout the study lifecycle. It offers hybrid work flexibility, with the potential for fully remote work for candidates with the right experience, and includes limited travel.
Key Responsibilities
- Provide medical management and expertise for clinical trials.
- Contribute medical input to study reports, regulatory documents, and manuscripts.
- Manage safety issues in clinical trials and support evaluation of trial data.
- Coordinate with cross-functional teams on feasibility, study design, educational efforts, and medical document review.
- Participate in proposal development and sponsor meetings to support new business efforts.
- Develop new clinical projects, including study design, protocol development, and project plans.
- Follow research protocols and support adherence to company policies.
Required
- Medical degree (M.D.).
- Therapeutic area specialization.
- Eligibility to obtain a medical license.
Preferred
- Board certification.
- Prior clinical trial research experience.
- Experience in pharmaceutical-related clinical research.
Benefits & Perks
- Hybrid work-from-home flexibility.
- Potential for fully remote work with the right experience.
- Travel up to 20%.
- Competitive compensation programs.
- Comprehensive health, wellness, retirement, and PTO benefits.
- On-site mentors and industry onboarding/training programs.
- Defined career paths with advancement opportunities.