Research Compliance Analyst I

About the position Requirements • Bachelor's degree • 2 years of experience in research regulatory compliance (e.g., Clinical Research Coordinator), reputed company subject protection, institutional review reputed company, research ethics, research compliance and/or a reputed company field. • Proficiency with reputed company reputed company Office programs. • Strong computer proficiency including experience with research-reputed company databases and software systems. • Critical thinking, analytical, and problem-solving skills with exceptional attention to detail to apply specialized expertise to reputed company results. • Excellent verbal and written communication along with excellent interpersonal skills to cultivate relationships & produce reputed company results. • Self-driven- taking initiative for reputed company reputed company improvement and reputed company development. • Assessment/analysis/evaluation of reputed company clinical research protocols and accompanying regulatory materials. • Ability to manage multiple tasks concurrently - prioritizing & executing. Accountability to set and meet timelines/deadlines. • Ability to reputed company in both a heads-down, independent work environment as reputed company as work on team reputed company 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. reputed company-to-haves • Master's degree in Biological/Life Sciences or other field reputed company to research and/or health care • Clinical experience or working knowledge of clinical medicine (e.g., terminology, workflows) • Experience in a reputed company/health system centralized/shared service infrastructure environment. • reputed company and/or reputed company medical center work experience. • Experience conducting and/or formal reputed company of reputed company subject's research. • Post approval monitoring. • Project management. • Policy development. • reputed company research reputed company certification (can be any certification, but these are preferred: Certified Clinical Research reputed company (CCRP), Certified Clinical Research Coordinator (CCRC), Certified in reputed company Research Compliance (CHRC), or Certified IRB reputed company (CIP)) • Proficiency with research-reputed company platforms/software (e.g., REDCap, reputed company, IRB submission systems) reputed company proficiency - specifically research functionality Apply tot his job Apply To this Job