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Research Compliance Specialist I

3 months ago

Chardon, United States University Hospitals Full time
What You Will Do
  • Conducts directed and prospective compliance reviews of research activities throughout the UH System, writes focused and timely reports, and ensure all reviews are appropriately completed. (60%)
  • Maintains current information regarding federal regulations, ethical considerations, UHCMC IRB and UH research polices related to the protection of human research participants and identifies opportunities for quality improvement. (15%)
  • Supports the research community in conducting research that is compliant with all applicable Federal and institutional policies; when there are allegations of non-compliance supports the investigative process. (25%)
Additional Responsibilities
  • Performs other duties as assigned.
  • Complies with all policies and standards.
  • For specific duties and responsibilities, refer to documentation provided by the department during orientation.
  • Must abide by all requirements to safely and securely maintain Protected Health Information (PHI) for our patients. Annual training, the UH Code of Conduct and UH policies and procedures are in place to address appropriate use of PHI in the workplace.


Qualifications:
Education
  • Bachelor's Degree (Required)
Work Experience
  • 1+ years experience in health related research (Required) and
  • Research monitoring or auditing experience (Preferred)
Knowledge, Skills, & Abilities
  • Strong clinical background with sound understanding of medical treatments, procedures, medications, etc. (Required proficiency)
  • Thorough understanding of responsible conduct of research and misconduct regulations. (Required proficiency)
  • Excellent interpersonal skills as well as professional conduct. (Required proficiency)
  • Good organizational and writing skills. (Required proficiency)
  • Computer skills (Microsoft Office). (Required proficiency)
Licenses and Certifications
  • Certification in Human Subjects Protection (CITI) within 30 Days (Required) and
  • Certified Clinical Research Coordinator (CCRC) Research Certification (CRA, CCRP, CIP) strongly encouraged. (Preferred)
Physical Demands
  • Standing Occasionally
  • Walking Occasionally
  • Sitting Constantly
  • Lifting Rarely 20 lbs
  • Carrying Rarely 20 lbs
  • Pushing Rarely 20 lbs
  • Pulling Rarely 20 lbs
  • Climbing Rarely 20 lbs
  • Balancing Rarely
  • Stooping Rarely
  • Kneeling Rarely
  • Crouching Rarely
  • Crawling Rarely
  • Reaching Rarely
  • Handling Occasionally
  • Grasping Occasionally
  • Feeling Rarely
  • Talking Constantly
  • Hearing Constantly
  • Repetitive Motions Frequently
  • Eye/Hand/Foot Coordination Frequently
Travel Requirements
  • 10%

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