Research Compliance Analyst I
About the position Requirements • Bachelor's degree • 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. • 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. Nice-to-haves • Master's degree in Biological/Life Sciences or other field related to research and/or health care • 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. • 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)) • Proficiency with research-related platforms/software (e.g., REDCap, Qualtrics, IRB submission systems) Epic proficiency - specifically research functionality Apply tot his job