CLINICAL RESEARCH COORD II

Temple University Health System • Philadelphia, PA

12h

About The Position

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.

Requirements

• Bachelor's Degree Required
• Combination of relevant education and experience may be considered in lieu of degree Required
• 2 years experience in a Clinical Research Coordinator role or 5 Years experience in related clinical research role Required
• CCRC, CCRP or ACRP-CP certification is required within 1 year from date of hire

Nice To Haves

• Master's Degree Preferred
• 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

Responsibilities

• Coordinates and facilitates the conduct of clinical research protocols
• Provides leadership in the management and operation of clinical research protocols
• Ensures research participant recruitment and accrual
• Ensures protocol compliance
• Ensures research participant safety and data quality
• Develops effective tools for close monitoring and reporting of trials accrual
• Coordinates the timely study activation and submission of protocol amendments
• Interacts with institutional investigators, healthcare team members, service line members and research participants/families

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level