Research Compliance Analyst III - Hybrid - 140948

About the role

The Research Compliance Analyst III serves as an experienced compliance professional supporting oncology research conducted within an academic medical center environment. The position independently conducts research compliance audits, reviews, consultations, investigations, and educational activities related to human subjects research and clinical trials. The incumbent applies knowledge of federal and state regulations, institutional policies, and industry best practices to identify compliance risks, evaluate processes, provide guidance to investigators and study teams, and promote responsible conduct of research. The position partners closely with research leadership, investigators, clinical research staff, and other institutional stakeholders to support compliance with regulatory requirements and strengthen the overall compliance program.

Responsibilities

• Conduct research compliance audits, reviews, consultations, investigations, and educational activities related to human subjects research and clinical trials.
• Apply knowledge of federal and state regulations, institutional policies, and industry best practices to identify compliance risks, evaluate processes, provide guidance to investigators and study teams, and promote responsible conduct of research.
• Partner with research leadership, investigators, clinical research staff, and other institutional stakeholders to support compliance with regulatory requirements and strengthen the overall compliance program.
• Work a hybrid schedule that includes onsite work at Greenwich Drive and remote work.
• Be able to work various hours and locations based on business needs.

Requirements

• Seven (7) years of related experience, education/training, OR a Bachelor’s degree in a related area plus three (3) years of related experience/training.
• Related experience includes research compliance, clinical research administration, human subjects protections, regulatory affairs, research quality assurance, healthcare compliance, clinical trial auditing, monitoring, research privacy, FDA‑regulated research, academic medical center compliance, or other experience interpreting and applying healthcare or research regulations and policies.
• Thorough knowledge of the methods, tools, and practices involved with regulatory compliance.
• Knowledge and understanding of compliance