Yale University
Research Associate 2
New Haven, Connecticut, 06510 · Principal · Contract
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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.
Responsibilities
- 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.
Requirements
- 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.
Compensation
- Required License(s) or Certification(s) Required License(s) or Certification(s): Physical Requirements Physical Requirements: Job Posting Date 06/01/2026 Job Category Professional Bargaining Unit NON Compensation Grade Clinical & Research C
This listing is sourced directly from Yale University's careers page and normalized into a canonical job model.