Senior Clinical Trial Ops: Start-Up & Compliance

relaytherapeutics; Cambridge (MA); On-site; USD 69,000 - 99,000; Full time

Job summary

Relay Therapeutics is seeking a Senior Clinical Project Associate to support end-to-end clinical trial coordination, from site start-up to study closure. You will work with CROs and vendors, maintain trackers, review essential documents, and help prepare meeting materials.

Strong communication, multitasking, and attention to detail are essential in our fast-paced environment. You should have 2–3 years of clinical trial experience, familiarity with GCP/ICH guidelines, and proficiency in MS Office

Qualifications

• 2–3 years of clinical trial experience.
• Familiarity with GCP and ICH guidelines and application to trials.
• Motivated self-starter in a fast-paced, small company.
• Strong communication and public speaking skills.
• Proficient with MS Office including MS Project, Excel and PowerPoint.

Responsibilities

• Coordinate day-to-day clinical trial execution across sites, CROs and vendors.
• Support site start-up, participant enrollment, monitoring and drug supply planning.
• Define clinical supply logistics and ensure GCP and protocol compliance.

Skills

Clinical trial coordination

GCP/ICH guidelines

MS Office (Projects, Excel, PowerPoint

Tools

MS Project

Excel

PowerPoint

Job description

Relay Therapeutics is seeking a Senior Clinical Project Associate to support end-to-end clinical trial coordination, from site start-up to study closure. You will work with CROs and vendors, maintain trackers, review essential documents, and help prepare meeting materials.

Strong communication, multitasking, and attention to detail are essential in our fast-paced environment. You should have 2–3 years of clinical trial experience, familiarity with GCP/ICH guidelines, and proficiency in MS Office