Research Protocol Analyst
A company is looking for a Research Protocol Analyst - Clinical Research Protections. Key Responsibilities Manage human research protocols through the review processes of relevant committees to ensure compliance with regulations Prepare materials for committee meetings and assist in audits to maintain protocol readiness Participate in quality improvement initiatives, including policy updates and workflow enhancements Required Qualifications Bachelor's degree with at least 2 years of experience in an academic/clinical research review setting, or 5 years of relevant experience in lieu of a degree Experience in the review and processing of research protocols in an academic research setting Knowledge of federal and state regulations regarding human and/or animal subjects in research Effective interpersonal skills for handling sensitive and confidential information Preferred certification as a Certified IRB Professional (CIP)
A company is looking for a Research Protocol Analyst - Clinical Research Protections.
Key Responsibilities
Manage human research protocols through the review processes of relevant committees to ensure compliance with regulations
Prepare materials for committee meetings and assist in audits to maintain protocol readiness
Participate in quality improvement initiatives, including policy updates and workflow enhancements
Required Qualifications
Bachelor's degree with at least 2 years of experience in an academic/clinical research review setting, or 5 years of relevant experience in lieu of a degree
Experience in the review and processing of research protocols in an academic research setting
Knowledge of federal and state regulations regarding human and/or animal subjects in research
Effective interpersonal skills for handling sensitive and confidential information
Preferred certification as a Certified IRB Professional (CIP)
