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Compliance Specialist, Healthcare

Job in Cambridge, Middlesex County, Massachusetts, 02140, USA
Listing for: Massachusetts Institute of Technology
Full Time position
Listed on 2026-01-30
Job specializations:
  • Healthcare
    Healthcare Nursing
Salary/Wage Range or Industry Benchmark: 60000 - 80000 USD Yearly USD 60000.00 80000.00 YEAR
Job Description & How to Apply Below

Overview

COMPLIANCE SPECIALIST 1, Vice President for Research, to ensure compliance with federal, state, and local policies, and guidelines related to research protocols involving human subjects at MIT on behalf of the Committee on the Use of Humans as Experimental Subjects (COUHES). The primary responsibility is to ensure that research protocols are clinically sound, ethical, and align with best practices, minimizing participant risk while ensuring standard of care, clear informed consent, and appropriate recruitment and screening.

Duties require on-campus presence to review study facilities and conditions.

Posting Date

12/15/2025

Qualifications
  • REQUIRED:

    Bachelor of Science in Nursing (BSN); current Massachusetts RN/NP license;
    National Board Certification (NP); minimum of five years of experience as nurse clinician and/or clinical nurse practitioner including involvement in clinical research; and familiarity with IRB processes and regulatory requirements.
  • PREFERRED:
    Master of Science in Nursing (MSN);
    Certification in Clinical Research (e.g., IACRN, CCRP, ACRP, SOCRA); understanding of relevant laws, guidelines, and ethical principles (e.g., 45 CFR Part 46, 21 CFR 50, 21 CFR 56, 21 CFR 812, 21 CFR 312, ICH-GCP); strong analytical and critical thinking skills; ability to assess research protocols and identify potential risks to human subjects; excellent communication and interpersonal skills; ability to communicate effectively with researchers, IRB members, and other stakeholders;

    ability to manage multiple projects and meet deadlines in a fast-paced environment; experience with research administration; and experience with FDA-regulatory and industry-sponsored trials.
Responsibilities
  • Ensure compliance with federal, state, and local policies and guidelines related to research involving human subjects.
  • Review study protocols to ensure clinical soundness, ethical considerations, informed consent clarity, appropriate recruitment and screening, and minimization of participant risk.
  • Collaborate with COUHES and researchers; participate in on-campus facility and condition reviews as required.

Full job description may be found at the original posting source.

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