Senior Clinical Trial Associate

We are seeking a detail-oriented, proactive Clinical Trial Associate with mid-senior level clinical operations experience. This role requires someone who can work independently, think critically, and seamlessly coordinate cross-functional study components in a fast-moving environment.

Drive toward study activation readiness by coordinating and executing key startup tasks across documentation, systems, and vendors

Own the setup of study tools, trackers, and operational workflows needed for a clean and efficient launch

Support clinical operations across study planning, execution, and vendor oversight

Draft and update key study documentation (e.g., study manuals, project plans, monitoring tools, training materials)

Oversee EDC and ePRO build and user acceptance testing (UAT); liaise with vendors as needed

Assist with data management tasks and ensure accuracy across systems and documents

Collaborate cross-functionally to ensure alignment and operational readiness

3–5 years of clinical trial experience at a sponsor (device experience preferred)

Prior experience supporting decentralized or hybrid trials

Strong working knowledge of EDC, ePRO, and clinical data workflows

Solid understanding of Good Clinical Practice (GCP) and applicable regulatory requirements (e.g., 21 CFR Parts 11, 50, 56, and 812)

Comfortable working autonomously with a high degree of ownership

Exceptional attention to detail with the ability to synthesize and manage operational complexity