Remote New

Clinical Research Data Coordinator

City of Hope
$24.81 - $40.90 / hr
United States
Jan 29, 2026
Clinical Research Data Coordinator About City of Hope, City of Hope's mission is to make hope a reality for all touched by cancer and diabetes. Founded in 1913, City of Hope has grown into one of the largest and most advanced cancer research and treatment organizations in the U.S., and one of the leading research centers for diabetes and other life-threatening illnesses. City of Hope research has been the basis for numerous breakthrough cancer medicines, as well as human synthetic insulin and monoclonal antibodies. With an independent, National Cancer Institute-designated comprehensive cancer center that is ranked top 5 in the nation for cancer care by U.S. News & World Report at its core, City of Hope's uniquely integrated model spans cancer care, research and development, academics and training, and a broad philanthropy program that powers its work. 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 cancer treatment centers and outpatient facilities in the Atlanta, Chicago and Phoenix areas. The successful candidate: Job Overview This position is responsible for the collection, coordination, processing and quality control of clinical trial data. This includes pre and post research activities, internal and external to the clinical setting. Responsible for implementation and conducting data management and compliance of multiple research projects. Job Responsibilities Review, synthesize and abstract information from medical records (clinic notes, pathology reports, radiology reports, patient questionnaires, etc.) to extract industry, cooperative, and investigator- initiated trial data as specified by research protocol into sponsor Electronic Data Capture (EDC) to support all research studies. Complete study visits and/or element completion in CTMS to correspond to EDC data entry. All data entry (EDC and CTMS) to be completed within 72 hours of study visit. Perform quality assurance checks to ensure the accuracy of data entered Work with providers/coordinators to identify and address data discrepancies and queries. Prepare documents and coordinate the study team, including principal investigators and pharmacists, for internal and/or external compliance monitor review/audit. Liaison between sponsored trial monitors and provider/coordinators. Work with providers to identify data points to answer queries and perform query function to export data requests. EDUCATION Minimumofanassociate degreeinlifesciencesorinformationsystemswithexperienceinthehealthfield preferred. 2-3 years clinical/oncology experience preferred City of Hope is an equal opportunity employer. To learn more about our comprehensive benefits, click here:Benefits Information City of Hope employees pay is based on the following criteria: work experience, qualifications, and work location.