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Research Compliance Specialist I
University Hospitals. Conduct directed and prospective compliance reviews of research activities throughout the UH System .
Core Competencies
Role fitCore Competencies
Use this summary to align your resume positioning with the role.
Demonstrates expertise in compliance reviews and research monitoring, with a strong understanding of federal regulations and ethical considerations in human research. Proficient in writing reports and maintaining compliance with institutional policies while supporting the research community.
Highest-signal resume keywords
Bachelor's Degree1+ Years Experience In Health Related ResearchCertification In Human Subjects Protection (CITI)Strong Clinical BackgroundResearch Monitoring Or Auditing Experience
ATS Keywords
Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills
Compliance ReviewsResearch MonitoringReport WritingUnderstanding Of Medical TreatmentsResponsible Conduct Of Research Regulations
Soft Skills
Excellent Interpersonal SkillsGood Organizational SkillsProfessional Conduct
Tools & Technologies
Microsoft Office
Certifications & Qualifications
Certification In Human Subjects Protection (CITI)Certified Clinical Research Coordinator (CCRC)Research Certification (CRA, CCRP, CIP)
Industry Keywords
Federal RegulationsEthical ConsiderationsHuman Research ParticipantsProtected Health Information (PHI)Quality Improvement
About the role
Key responsibilities & impact- Conduct directed and prospective compliance reviews of research activities throughout the UH System
- Write focused and timely reports
- Ensure all reviews are appropriately completed
- Maintain current information regarding federal regulations, ethical considerations, UHCMC IRB and UH research policies related to protecting human research participants
- Identify opportunities for quality improvement
- Support the research community in conducting compliant research under applicable federal and institutional policies
- Support investigative processes when there are allegations of non-compliance
- Perform other duties as assigned
Requirements
What you’ll need- Bachelor's Degree (Required)
- 1+ years experience in health related research (Required)
- Research monitoring or auditing experience (Preferred)
- Strong clinical background with sound understanding of medical treatments, procedures, medications, etc.
- Thorough understanding of responsible conduct of research and misconduct regulations
- Excellent interpersonal skills and professional conduct
- Good organizational and writing skills
- Computer skills (Microsoft Office)
- Certification in Human Subjects Protection (CITI) within 30 Days (Required)
- Certified Clinical Research Coordinator (CCRC) Research Certification (CRA, CCRP, CIP) strongly encouraged (Preferred)
- Must comply with policies and standards
- Must safely and securely maintain Protected Health Information (PHI)
- Ability to travel 10% of the time
Benefits
Comp & perks- Annual training
- UH Code of Conduct and UH policies and procedures addressing appropriate use and secure maintenance of Protected Health Information (PHI)