Overview

In 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 / Benefits

- Flexible 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

Responsabilità

- Provide 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 fondamentali

- 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

- 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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