Research Protocol Analyst (Remote)

Join the forefront of groundbreaking research at the

where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. Our dedicated and compassionate faculty and staff are driven by a common mission: Contribute to innovative approaches in predicting, preventing, and curing diseases, shaping the future of medicine through cutting-edge research.

Clinical Research Protections provides support to the Data and Safety Monitoring Committee (DSMC). Research Protocol Analysts oversee human research protocols, ensuring compliance with federal regulations and cancer center grant requirements. They serve as resources for City of Hope researchers and committee members, interacting regularly with Principal Investigators, study teams, and other departments involved in research at City of Hope facilities. In this dynamic environment, their dedication ensures that every research protocol is executed with precision, integrity, and utmost ethical consideration.

As a successful candidate, you will:

• Oversee the management of research protocols throughout the Data and Safety Monitoring Committee (DSMC) review process to ensure compliance with regulations.
• Conduct pre-reviews of submissions, ensuring completeness and compliance, coordinating timely reviews, preparing committee minutes, and issuing action notices to investigators summarizing review outcomes.
• Monitor investigator responses and progress reporting, providing assistance and escalating issues when necessary.
• Prepare materials for committee meetings, offer guidance on novel regulatory questions, and address member inquiries.
• Assist in preparing for audits, ensuring protocol documentation meets internal and external requirements.
• Identify areas for process improvement and regulatory compliance, staying updated on regulations and participating in quality improvement initiatives and educational sessions as required.

Your qualifications should include:

• Bachelor's degree.
• At least 2 years of experience in the academic/clinical research review setting.

Preferred qualifications:

• Certified IRB Professional (CIP), Certified Clinical Research Professional (CCRP), or Certified Clinical Research Coordinator (CCRC).
• Experience in review and processing of research protocols in an academic research setting.

City of Hope is an equal opportunity employer. To learn more about our commitment to diversity, equity and inclusion, please click here.