Clinical Research Regulatory Coordinator - Oncology

About the role

This position independently manages and coordinates all aspects of clinical trials for selected departments and populations in accordance with regulatory and institutional guidelines, working closely with research management and the Principal Investigator. It also oversees the implementation of research trials to ensure compliance with federal and institutional requirements.

Key responsibilities

• Manages research activities associated with clinical trials and data management and facilitates successful study start‑up.
• Maintains study compliance, ensures compliance with regulatory guidelines, and participates in internal and external audits.
• Manages data and leads special projects and tracks project progress.
• Maintains strong relations with study sponsors.
• Seeks opportunities for individual and departmental continuing education.
• Performs other related duties as assigned.

Required profile

• High school diploma or equivalent.
• Three years of relevant research experience in a clinical setting, or two years with ACRP or SOCRA certification.
• Strong critical thinking skills and solid knowledge of medical and clinical research terminology and processes.
• Knowledge of safe protocol management in clinical trials.
• Ability to coordinate and oversee regulatory processes throughout the trial lifecycle.
• Effective verbal and written communication skills with the ability to present information clearly to diverse audiences.