Yale University

Research Associate 2

New Haven, Connecticut, 06510 · Principal · Contract

Sponsorship not specified$65k-$101kDetected 51 days ago

GCPAccessibilityClinical TrialsClinical ResearchResearchGxP

About the role

Working at Yale means contributing to a better tomorrow.
This includes coordinating and scheduling adjudication meetings, communicating with CEC members, and escalating endpoint or adjudication-related issues to appropriate stakeholders.
The role is responsible for collecting and assembling source documentation for suspected clinical endpoints, preparing complete and appropriately blinded endpoint packets, and ensuring readiness for committee review.

For additional information on the background check requirements and process visit "Learn about background checks" under the Applicant Support Resources section of Careers on the It's Your Yale website.
Overview The Research Associate supports the formation and administrative operations of the Clinical Events Committee (CEC) within a clinical research environment.
The Research Associate drafts and reviews clinical event narratives, performs data verification, and may track clinical events, maintain study master files, and develop templates to support efficient workflows.
Depending on study needs, the Research Associate may perform additional functions such as problem and safety coordination activities, while ensuring adherence to Good Clinical Practice (GCP) and study protocols.

These may include vaccinations, tests, or examinations, as required by law, regulation, or university policy.
Required Skills and Abilities 1.
Strong understanding of clinical research processes, including clinical trials and endpoint adjudication.

This listing is sourced directly from Yale University's careers page and normalized into a canonical job model.