14 set - Monza
Medpace
Overview
In this role you lead medical, scientific, and strategic direction for clinical trials and act as the internal medical expert for study results. You will shape study design, protocols, and project plans while ensuring rigorous evaluation and reporting. You collaborate across departments and with sponsors to support proposal development and trial execution. You will help translate findings into regulatory and scientific documents, guiding safety and interpretation of results. This position offers hybrid WFH flexibility and an opportunity to impact multiple therapeutic areas.
Retribuzione / Benefits
- Flexible work environment
- Competitive compensation and benefits
- 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 and collaborate on evaluation of trials
- Participate in new business development through proposals and sponsor meetings
- Coordinate with other departments across all study phases, including feasibility, design, education, medical information, and document review
- Ensure adherence to research protocols and policies
Requisiti fondamentali
- MD degree or equivalent
- Board certification and current medical licensure preferred
- Prior clinical trial research experience preferred
- Experience in pharmaceutical-related clinical research preferred
- leadership
- cross-functional collaboration
- effective communication
- clinical trial management
- study design and protocol development
- safety management / pharmacovigilance
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