Clinical Trials Data Coord

About the role

Clinical Trials Data Coordinator - Remote 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. Our dedicated and compassionate employees are driven by a common mission: To deliver the cures of tomorrow to the people who need them today. This full-time remote position entails ensuring data integrity for various research studies.

Responsibilities

• Data abstraction
• CRF completion
• Query resolution
• Sponsor monitor visit coordination
• Maintaining audit-ready data
• Oversee electronic research records and patient information in the CTMS, contributing to cutting-edge clinical research
• Possess in-depth knowledge of Good Clinical Practices (GCP), Food and Drug Administration (FDA) regulations, NIH guidelines, and HIPPA regulations
• Collaborate effectively as a valuable member of the clinical research team, demonstrating clear and timely written and verbal communication skills, including the sharing of critical information
• Take responsibility for communicating any protocol deviations or issues related to study execution, ensuring transparency and problem resolution
• Maintain strict adherence to study protocols by comprehending, communicating, and overseeing the proper execution of study parameters in accordance with protocol requirements
• Seek appropriate supervision, when necessary, prioritize tasks effectively, consistently meet deadlines, and exhibit meticulous attention to detail in all aspects of your work

Qualifications

• Bachelor’s Degree (relevant experience may substitute for degree)
• At least two years of experience related to the conduct of oncology clinical trials
• Working knowledge of clinical trials, Federal, State, and Local Regulations, and IRB requirements