Clinical Study Coordinator

City of Hope•Newnan, GA

1d•Onsite

About The Position

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. Under direct supervision of the Director, Clinical Research and/or Research Manager, the incumbent is responsible for supporting clinical trials at the top of their scope, for existing and novel oncology therapies while working in a fast-paced environment. Trial responsibility ranges from First in Human and Phase I-Phase III clinical trials, in addition to Therapeutic Investigator Initiated Trials (IIT’s). The Clinical Study Coordinator (“Study Coordinator") position has a specific responsibility for all aspects of coordination of therapeutic trials in the various oncology disease areas supported at the site.

Requirements

Bachelor’s degree in Science, Health or related field from an accredited university; 3 additional years of experience plus the minimum experience requirement may substitute for minimum education
Minimum of 2 years research or relevant clinical experience
ACRP or SOCRA certification within 1 year of employment
International Air Transport Association (IATA) within 1 month of employment
Good Clinical Practice (GCP) within 1 month of employment
Human Subjects Protection (HSP) within 1 month of employment
Basic Life Support (BLS) within 1 month of employment

Nice To Haves

Minimum 3+ years of oncology experience
Phase 1 clinical trial experience

Responsibilities

Support clinical trials for existing and novel oncology therapies
Coordinate First in Human and Phase I-Phase III clinical trials
Coordinate Therapeutic Investigator Initiated Trials (IIT’s)
Coordinate all aspects of therapeutic trials in various oncology disease areas supported at the site