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Salary: USD 69,000 - 99,000 / annual
Relay Therapeutics, a clinical-stage precision medicines company, is seeking a Senior Clinical Project Associate to support the execution of clinical trials. You will be an integrated member of the Clinical Development Operations team, accountable for clinical trial coordination and implementing operational plans in accordance with regulatory guidelines and ICH/GCP standards.
Key responsibilities include:
- Support day-to-day clinical trial operations, including site start-up, participant enrollment, clinical monitoring, drug supply planning and logistics, and GCP/protocol compliance across clinical sites, CROs, and vendors
- Coordinate with the CRO and Clinical Operations Lead to support planning from study initiation through closure
- Maintain study trackers and provide metrics as needed
- Review and contribute to key study documents including informed consent forms, case report forms, and study plans
- Prepare and distribute meeting agendas and minutes; actively participate in team meetings with updates on key responsibilities
- Ensure the Trial Master File is up-to-date and inspection-ready
- Support inspection readiness by collaborating with CROs and clinical sites to prepare for and respond to audit/inspection findings from internal QA and external regulatory agencies
- Actively participate in department initiatives and contribute ideas to improve efficiency and effectiveness of Clinical Operations
Relay Therapeutics is transforming drug discovery through insights into protein motion and dynamic behavior. The company's Dynamo platform integrates experimental and computational approaches to drug previously intractable protein targets, with an initial focus on targeted oncology. The team is collaborative, intellectually stimulating, and driven by a passion for bringing life-changing therapies to patients.
Requirements:
- 2-3 years of clinical trial experience; CRO or Sponsor experience strongly preferred
- Familiarity with GCP and ICH Guidelines and their application to clinical trial conduct
- Motivated self-starter capable of thriving in a fast-paced, small company environment
- Creative problem-solver with excellent communication and public speaking skills
- Proficiency with MS Office products (MS Project, Excel, PowerPoint)
- Strong interpersonal and organizational skills with high attention to detail
- Ability to manage multiple projects and needs effectively in a pragmatic manner
