EXTRAMURAL CLIN RESEARCH COORD

Temple University Health SystemPhiladelphia, PA
2d

About The Position

This position supports the Fox Chase Cancer Center Office of Clinical Research at Temple University Hospital, Main Campus or East Norriton and Buckingham Campuses. Coordinates and facilitates the conduct of clinical research protocols, which includes the collection and handling of research specimens, documentation and shipment following IATA guidelines. 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. Coordinates data management for satellite location. 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. IATA Certification class will be provided within 3 months from date of hire.

Requirements

  • Bachelor's Degree Required
  • 2 years experience in a healthcare setting preferably oncology or clinical trials Required

Nice To Haves

  • Graduate Level Classes or Degree in a relevant program Preferred or Combination of relevant education and experience may be considered in lieu of degree Required
  • 2 years experience with oncology clinical trials Preferred
  • 1 year experience performing phlebotomy and specimen processing Preferred
  • General Experience and knowledge of chemotherapy and/or radiation therapy administration Preferred
  • Cert Clin Research Coordinator Preferred
  • Cert Clin Research Prof Preferred
  • Cert Clin Research Associate Preferred

Responsibilities

  • Coordinates and facilitates the conduct of clinical research protocols
  • Collection and handling of research specimens
  • Documentation and shipment following IATA guidelines
  • Provides leadership in the management and operation of clinical research protocols
  • Ensure research participant recruitment and accrual
  • Ensure protocol compliance
  • Ensure research participant safety and data quality
  • Coordinates data management for satellite location
  • 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.
  • Maintain flexibility in work schedule when possible to ensure coverage of study responsibilities.
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