14 set - Varese
Medpace
OverviewIn 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 / BenefitsFlexible 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
ResponsabilitàProvide 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 fondamentaliMD 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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