OverviewIn this role you will provide medical leadership for clinical trials and serve as the internal medical expert for study reports and regulatory documents.
You will guide study design and project plans while ensuring safety and scientific integrity across trials.
You'll collaborate with cross-functional teams and support business development through sponsor interactions.
The position offers hybrid WFH flexibility and a chance to shape trial strategy and execution in a global CRO setting.
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 trials and coordinate evaluation with team members
Participate in new business development through proposals and sponsor meetings
Coordinate with departments across feasibility, design, education, medical information, and document review/editing
Ensure strict adherence to research-related protocols and policies
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
leadership and able to coordinate across functions
strong communication and collaboration
attention to compliance and meticulousness
medical management of clinical trials
safety monitoring in trials
study design and protocol development

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