Employer Industry: Research and Healthcare

Why consider this job opportunity:
- Opportunity for career advancement and growth within the organization
- Engaging work that supports the Human Research Protection Program
- Comprehensive involvement in quality assurance reviews and audits of research studies
- Chance to collaborate with Investigators and study staff for compliance improvements
- Strong focus on education and process development in research practice

What to Expect (Job Responsibilities):
- Conduct ongoing quality assurance reviews and audits of research studies
- Assess site readiness and develop site-specific education and processes
- Ensure compliance with federal, state laws, and employer requirements
- Identify opportunities to improve processes, education, and compliance related to research practice
- Collaborate with clinical research monitors or auditors on various research studies

What is Required (Qualifications):
- Bachelor’s degree in an appropriate field (nursing, science, or health-related management)
- Minimum of three (3) years of experience in an IRB Human Subject Protection role or clinical research
- Certification as CIP, CCRC, CCRP, CQA, or CQAP, or must be obtained within two (2) years of eligibility
- Current state of Florida Registered Nurse (RN) licensure (active, eligible, or retired)
- Relevant field experience can be considered in lieu of degree requirement on a year-for-year basis

How to Stand Out (Preferred Qualifications):
- Past auditing experience or similar quality assurance activities related to clinical trials
- Knowledge of Federal regulations related to human subject protection, e.g., DHHS, FDA
- Strong verbal, written, and interpersonal communication skills
- Excellent organizational, critical thinking, and problem-solving skills
- Proficiency in Microsoft Office, including Word, Excel, PowerPoint, and familiarity with IRBNet.org

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