Assoc Clinical Research Coord

About the role

Join the transformative team at City of Hope, where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope’s growing national system includes its Los Angeles campus, a network of clinical care locations across Southern California, a new cancer center in Orange County, California, and treatment facilities in Atlanta, Chicago and Phoenix.

Responsibilities

• Ensure adherence to protocol for specimen collection and sponsor-specific equipment procedures, guaranteeing accurate documentation.
• Identify and promptly communicate important protocol and data management issues to the supervisor.
• Uphold Good Clinical Practices, FDA Rules, NIH guidelines, HIPAA regulations, ICH guidelines, and institutional policies for clinical trials.
• Enter accurate and up-to-date data into the clinical research management system (CRMS) for study patients.
• Collaborate within the clinical research team, maintaining positive and effective communication while seeking ways to improve job performance and surroundings.

Qualifications

• Bachelor’s degree.
• Experience may substitute for minimum education requirements. (Associate Degree plus minimum of 2 years of experience).
• At least one year of experience related to the management and conduct of oncology clinical trials in an academic setting, or six months experience as a Project Coordinator or Biospecimen Coordinator in the CTO.
• Working knowledge of clinical trials, Federal, State, and Local Regulations, IRB requirements, consent form and protocol development.
• Good Clinical Practice (GCP) and Health Information Portability and Accountability ACT (HIPAA)-to be provided by COH if not already completed.