15 set - Pavia
Medpace
Overview
In this role you will provide medical leadership for clinical trials, guiding scientific strategy, trial execution, and reporting. You will serve as the internal medical expert for study results interpretation and contribute to protocol and project design. You will collaborate with cross-functional teams to manage safety, regulatory documents, and manuscripts, and participate in business development as needed. The position offers hybrid work flexibility and opportunities to influence trial design and medical strategy within a biotech/pharma CRO environment. This role appeals to a physician who wants to shape clinical programs and drive meaningful therapeutic work.
Retribuzione / 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
Responsabilità
- Provide medical management and expertise for clinical trials
- Contribute medical input to study reports,
regulatory documents, and manuscripts
- Manage safety issues in clinical trials in collaboration with the team
- Participate in business development through proposal and sponsor meetings
- Coordinate with other departments across feasibility, design, medical information, and document review/editing
- Lead adherence to research protocols and policies
- Influence study planning, protocol development, and project plans
Requisiti fondamentali
- MD degree or equivalent
- Board certification and current medical licensure preferred
- Prior clinical trial research experience preferred
- Previous experience in pharmaceutical-related clinical research preferred
- collaboration and cross-functional teamwork
- clear scientific communication
- problem-solving and risk assessment
- clinical trial management
- study design and protocol development
- regulatory document preparation and review
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