Clinical Project Associate

As Clinical Project Associate, you will be accountable for providing clinical trial coordination support, along with implementing operational plans in accordance with regulatory guidelines and ICH/GCP standards. You will be an integral member of the Relay Tx Clinical Development Operations team making key contributions to the execution of clinical trials that will translate Relay’s innovative science into impactful medicines for patients.

• Partner with Clinical Project Managers to support day‑to‑day operations of clinical trial execution, focusing on site start‑up, study participant enrollment, clinical monitoring, GCP and protocol compliance for sites, CROs, and vendors.
• Serve as the point of contact for CROs, vendors, investigators, and clinical site staff to support trial deliverables, effective communication, and strong working relationships.
• 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 including training records, regulatory packets, informed consent forms, case report forms, study oversight committee charters, and study plans.
• Maintain version control and documentation across clinical materials.
• Coordinate and track trial‑specific equipment and supplies as appropriate.
• Coordinate trial team meetings, including schedules, distribution, agendas, minutes, and action items, and actively participate in meetings providing updates on key responsibilities.
• Help ensure the Trial Master File (TMF) is up‑to‑date and inspection ready.
• Support inspection readiness by collaborating with CROs and helping clinical sites prepare for and respond to audit/inspection findings conducted by internal QA and external regulatory agencies.
• Actively participate in the development of department initiatives and contribute ideas to improve the efficiency and effectiveness of Clinical Operations.

• Bachelor’s degree with at least 2+ years of relevant clinical trial experience (e.g., CRO, sponsor, clinical site, or clinical trial vendor).
• Familiarity with GCP and ICH Guidelines and their application to the conduct of clinical trials.
• Motivated self‑starter capable of thriving in a fast‑paced small company environment.
• Creative problem‑solver with excellent communication and public speaking skills.
• Proficient with MS Office products (MS Project, Excel, PowerPoint).
• Strong interpersonal and organizational skills, with a high degree of attention to detail.
• Pragmatic with proven ability to manage multiple competing tasks and demands.

Estimated Salary Range
: $61,000 - $87,000.

Relay Therapeutics is a clinical‑stage precision medicines company transforming the drug discovery process with the goal of bringing life‑changing therapies to patients.

As set forth in Relay Therapeutics’s Equal Employment Opportunity policy, we do not discriminate on the basis of any protected group status under any applicable law.