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

📌 Medical Director (Varese)
🏢 Medpace
📍 Varese