Research Fellow (Clinical Trials)

Valhalla, NYFull-timePosted Apr 30, 2026

Behavioral Health Market Context

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•Qualifications/Requirements Experience: 2-3 years of research or regulatory experience in an academic research setting
•Bachelors degree

•The regulatory specialist will be responsible for submitting protocols and supporting documents to regulatory bodies, including the Medical Executive Committee and IRB
•Responsibilities Submit continuations, amendments, generate reports, and maintain research files, including training and delegation logs consistent with the regulatory requirements for research studies/clinical trials, ensuring compliance with all federal and local agencies, including the FDA and local IRB
•Will attend team meetings, work with other staff to ensure all regulatory documents and requirements are met and up-to-date
•Provide strategies for improving efficiency and quality
•May represent investigators when meeting with pharmaceutical companies as needed
•2 more items(s)