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Yale University

Research university in New Haven, CT

Regulatory Affairs Analyst

Full-TimeUpdated on 10/15/2026
$55k - $85k
Junior
Bachelor's
New Haven, CT, USA
In Person
Biology & BiotechClinical Research Operations

About the job

Requirements
  • Demonstrated experience and understanding with Institutional Review Board (IRB) protocols and submissions.
  • Professional verbal and written communication skills, including the ability to share knowledge and communicate complex ideas across cross-functional teams.
  • Proficient computer skills and working knowledge of the Microsoft Office suite, with the ability and desire to learn new computer platforms and software programs.
  • Ability to work independently, prioritize tasks with competing deadlines, and work with minimal supervision.
  • Attention to detail, organizational and time management abilities, and the ability to manage multiple concurrent projects while balancing priorities and timelines.
  • A bachelor's degree in a related field and one year of related work experience in the same job family, or an equivalent combination of experience and education.
  • Knowledge of regional and federal regulations and the ability to make independent decisions daily.
Responsibilities
  • Provide regulatory affairs support for clinical trials in the Gynecologic Oncology Division Clinical Trials Office, including setting up, activating, and supporting investigator-initiated, federally funded, and industry-sponsored protocols.
  • Prepare and submit initial protocol, amendment, and continuing review submissions to the Protocol Review Committee, Institutional Review Board, and ancillary committees.
  • Track evidence of protocol- and Institutional Review Board-required training for research staff.
  • Maintain and share regulatory files with study sponsor monitors, auditors, and inspectors to ensure compliance with protocol requirements, university procedures, and applicable authorities.
  • Receive and track safety reports; collaborate with Clinical Trials Office staff, laboratory staff, and pharmacy staff regarding study status changes; and liaise between the Clinical Trials Office, research staff, and study sponsors about regulatory matters.
  • Work with investigators and study team members, including project managers, on small projects or sections of medium projects to consult, conduct analysis, and identify trial objectives and requirements within defined parameters.
  • Interpret research business needs and translate them into application and operational requirements for research areas; develop tools and workshops to elicit requirements.
  • Evaluate information from research protocols, clinical trial agreements, and research financial budgets and fees, reconcile conflicts, and decompose high-level information into data essentials.
  • Analyze data using standard methods, interpret results, and prepare written summaries and data-analysis reports; develop reporting modules, ad hoc reports, and related reporting tools; and conduct research, data analysis, modeling, projecting, and scenario analyses using planning technology and databases.
  • Develop and maintain documentation and libraries on key processes.
  • Assess risk and ensure compliance with research protocols and guidelines, university procedures, and third-party regulations.
  • Determine training needs and design, develop, and conduct training sessions, meetings, and conference calls with study teams and staff members.
  • Perform or assist with research compliance audits or self-assessments.
  • Communicate perspectives on business opportunities, needs, and risks.
Desired Qualifications
  • Demonstrated experience supporting an oncology department.
  • Demonstrated experience as a clinical research analyst supporting regulatory affairs.

About the company

Yale University is a private research university in New Haven, Connecticut. It provides undergraduate, graduate, and professional education alongside research, scholarship, and public engagement.

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