Research Compliance Analyst
Listed on 2026-09-18
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Healthcare
Clinical Research, Medical Science
Total Rewards
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Expected pay for this position is $33.52 - $42.40/hour. Actual pay will be determined by experience, skills and internal equity. This is a Salaried position.
OverviewPlease Note:
This is position is not eligble for H1B Sponsorship.
The Research Compliance Analyst II (RCA) is a research administration and oversight professional with subject matter expertise and proficiency in human subject protections and research administration. The RCA II is responsible for ensuring institutional due diligence in compliance with regulations, laws, ethical principles and professional standards that govern the conduct of human subject research at OSF Health Care. The RCA II performs comprehensive analysis, develops and provides educational & consultative support, and develops and contributes to continuous quality assurance & improvement efforts to maintain ethical standards and regulatory compliance.
The RCA II acts as a liaison between research teams, the institution(s), and the Institutional Review Boards (IRBs), safeguarding the interests of all parties & participants involved in the conduct and oversight of human subject research. The RCA II must exhibit a moderate level of expertise in the conceptualization and conduct of clinical and non-clinical research (i.e., protocol development and scientific method, data management, funding and billing), and must perform job duties with a level of independence that warrants minimal direction.
RCA I REQUIRED QUALIFICATIONS
Education:
Bachelor’s degree
Experience:2 years of experience in research regulatory compliance (e.g., Clinical Research Coordinator), human subject protection, institutional review board, research ethics, research compliance and/or a related field.
Other Skills/ Knowledge:- Proficiency with all Microsoft Office programs.
- Strong computer proficiency including experience with research-related databases and software systems.
- Critical thinking, analytical, and problem-solving skills with exceptional attention to detail to apply specialized expertise to achieve results.
- Excellent verbal and written communication along with excellent interpersonal skills to cultivate relationships & produce optimal results.
Education:
Bachelor’s degree
Experience:4 years of experience in research regulatory compliance (e.g., Clinical Research Coordinator), human subject protection, institutional review board, research ethics, research compliance and/or a related field
Licensure/ Certification:Current research professional certification (Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), Certified in Healthcare Research Compliance (CHRC), or Certified IRB Professional (CIP))
Other Skills/Knowledge:- Clinical experience or working knowledge of clinical medicine (e.g., terminology, workflows).
- Proficiency with all Microsoft Office programs. Strong computer proficiency, including experience with research-related databases and software systems.
- Critical thinking, analytical, and problem-solving skills with exceptional attention to detail to apply specialized expertise to achieve results.
- Excellent verbal and written communication along with excellent interpersonal skills to cultivate relationships & produce optimal results.
- Self-driven & independent– taking initiative for continuous quality improvement and professional…
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