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About the Role

Manage clinical research projects, ensuring adherence to ethical guidelines and regulations. Oversee project structures, develop study plans, manage timelines, control documentation, budgets, and coordinate cross-functional teams. Serve as the primary contact for vendors and clients.

Responsibilities

• Build and oversee project structures
• Develop study plans, including risk management plans
• Manage timelines and milestones
• Control documentation, budgets, and invoicing
• Coordinate cross-functional teams
• Serve as the primary contact for vendors and clients

Requirements

• Project management experience in clinical or real-world evidence research
• Full understanding of the study process from planning to publication
• Proven ability in progress tracking and cross-department coordination
• Strong proposal and negotiation skills
• Expertise in a specific disease area
• English proficiency (reading and writing required; speaking preferred)