Clinical Research Coord

Fox Chase Cancer Center • Philadelphia, PA

1d • Onsite

About The Position

Temple Health is a dynamic network of outstanding hospitals, specialty centers, and physician practices, including Temple University Hospital (TUH), Fox Chase Cancer Center, and other campuses. It is affiliated with the Lewis Katz School of Medicine at Temple University and is committed to advancing the fight against disease, medical science, and educating future healthcare professionals. The organization recruits top talent to its diverse 10,000-strong workforce, fostering a healthy, safe, and productive environment. This Clinical Research Coordinator position involves coordinating and facilitating clinical research protocols supported by various entities like NCI, industry, cooperative groups, or grants. The role provides leadership in managing and operating these protocols to ensure participant recruitment, protocol compliance, safety, and data quality. The coordinator will collaborate with the clinical research team to develop tools for monitoring trial accrual and coordinate timely study activation and amendment submissions. This role specifically supports the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses, requiring interaction with investigators, healthcare team members, service line members, and research participants/families to support clinical trials. Flexibility in work schedule is essential to ensure coverage of study responsibilities.

Requirements

• Bachelor's Degree Required
• 2 years direct experience in a healthcare setting preferably oncology or clinical trials or a minimum of 3 Years related experience Required

Nice To Haves

• Graduate Level Classes or Degree in a relevant program Preferred
• Combination of relevant education and experience may be considered in lieu of degree
• General Experience and knowledge of chemotherapy and/or radiation therapy administration Preferred
• Previous experience performing phlebotomy and specimen processing Preferred
• Cert Clin Research Coordinator Preferred
• Cert Clin Research Prof Preferred
• Assn Clin Res Prof - Cert Prof Preferred

Responsibilities

• 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.
• Work closely with the members of the clinical research team to develop effective tools for close monitoring and reporting of trials accrual.
• Coordinate the timely study activation and submission of protocol amendments.
• 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.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level
• Number of Employees: 501-1,000 employees