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.





Retribuzione / Benefits Flexible work environment Competitive compensation and benefits package Competitive PTO packages Structured career paths with opportunities for professional growth Employee health and wellness initiatives 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 Coordinate with other departments across feasibility, design, medical information, and document review/editing Influence study planning, protocol development, and project plans 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 clinical trial management regulatory document preparation and review

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