Research Compliance Analyst I
US-IL-Peoria
External Apply Portal
Req #: 87996
Type: Full Time
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Overview: Please note: H-1B sponsorship is not offered for this opening(s). ***This position is a Hybrid schedule at OSF HealthCare Ministry Headquarters in Peoria, IL.** POSITION SUMMARY: The Research Compliance Analyst I (RCA) is a research administration and oversight professional with subject matter expertise in human subject protections. The RCA I 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 HealthCare. The RCA I performs comprehensive analysis, provides educational & consultative support, and contributes to continuous quality assurance & improvement efforts to maintain ethical standards and regulatory compliance. The RCA I 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. Qualifications: 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. * Self-driven- taking initiative for continuous quality improvement and professional development. * Assessment/analysis/evaluation of complex clinical research protocols and accompanying regulatory materials. * Ability to manage multiple tasks concurrently - prioritizing & executing. Accountability to set and meet timelines/deadlines. * Ability to thrive in both a heads-down, independent work environment as well as work on team projects collaboratively. * Understanding of the multiple regulatory frameworks governing conduct of research (e.g., OHRP, FDA, HIPAA, NIH). * Understanding of regulations and their application in research. PREFERRED QUALIFICATIONS: Education: Master's degree in Biological/Life Sciences or other field related to research and/or health care Experience: * Clinical experience or working knowledge of clinical medicine (e.g., terminology, workflows) * Experience in a healthcare/health system centralized/shared service infrastructure environment. * Academic and/or academic medical center work experience. * Experience conducting and/or formal oversight of human subject's research. * Post approval monitoring. * Project management. * Policy development. Licensure/ Certification: Current research professional certification (can be any certification, but these are preferred: Certified Clinical Research Professional (CCRP), Certified Clinical Research Coordinator (CCRC), Certified in Healthcare Research Compliance (CHRC), or Certified IRB Professional (CIP)) Other Skills/ Knowledge: Proficiency with research-related platforms/software (e.g., REDCap, Qualtrics, IRB submission systems) Epic proficiency - specifically research functionality OSF HealthCare is an Equal Opportunity Employer.
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