Clinical Research Coordinator II

Coordinates and facilitates the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. Provides leadership in the management and operation of clinical research protocols to ensure research participant recruitment and accrual, protocol compliance, research participant safety and data quality. The position will work closely with the members of the clinical research team to develop effective tools for close monitoring and reporting of trials accrual and coordinate the timely study activation and submission of protocol amendments. This position supports the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses. In addition, this position is expected to interact with the institutional investigators, other members of the healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials. Flexibility in work schedule, when possible, must be maintained to ensure coverage of study responsibilities. CCRC, CCRP or ACRP-CP certification is required within 1 year from date of hire.

Education
Bachelor's Degree Required
Master's Degree Preferred or
Combination of relevant education and experience may be considered in lieu of degree Required

Experience
2 years experience in a Clinical Research Coordinator role or 5 Years experience in related
clinical research role Required
2 years experience with oncology clinical trials Preferred
General Experience and knowledge of chemotherapy and/or radiation therapy

administration Preferred
General Experience Previous experience performing phlebotomy and specimen processing Preferred

Licenses
Cert Clin Research Coordinator Required or
Cert Clin Research Prof Required or
Assn Clin Res Prof - Cert Prof Required