Associate Clinical Project Manager

The Associate Clinical Project Manager will support clinical studies that lead the biopharma industry in speed and quality of clinical study design and execution. The role will involve day-to-day operations, site oversight, vendor management, and ensuring quality data delivery.

Requirements

• 5+ years of experience in clinical study management
• Sponsor experience strongly preferred
• Strong knowledge of global regulatory and compliance requirements
• Experience in executing clinical studies across various phases
• Expertise in oncology drug development preferred
• Ability to flourish in a fast-paced small company environment

Benefits

• Generous Paid Time Off
• 401k Matching
• Retirement Plan
• Visa Sponsorship