Clinical Project Associate

Responsibilities

• Partner with Clinical Project Managers to support day-to-day clinical trial execution, including site start-up, enrollment, and monitoring
• Serve as a point of contact for CROs, vendors, investigators, and clinical site staff
• Develop, maintain, and improve study tracking tools
• Assist with vendor and site invoice review, budget management, and tracking
• Review and contribute to key study documents such as training records, regulatory packets, and informed consent forms
• Maintain version control and documentation across clinical materials
• Coordinate trial team meetings, including agendas, minutes, and action items
• Ensure the Trial Master File (TMF) is up-to-date and inspection ready
• Support inspection readiness by collaborating with CROs and clinical sites for audits

Requirements

• Bachelor’s degree
• 2+ years of relevant clinical trial experience (CRO, Sponsor, clinical site, or vendor)
• Familiarity with GCP and ICH Guidelines
• Proficiency with MS Office (MS Project, Excel, and PowerPoint)
• Strong interpersonal, organizational, and communication skills
• Ability to manage multiple competing tasks in a fast-paced environment

About the Company

Relay Therapeutics is a clinical-stage precision medicines company transforming the drug discovery process. Built on insights into protein motion, the company aims to bring life-changing therapies to patients, with an initial focus on targeted oncology.