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Extramural Clinical Research Coord at Temple Health System

Philadelphia, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

01 Jan, 26

Salary

0.0

Posted On

03 Oct, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Data Management, Phlebotomy, Specimen Processing, Oncology, Protocol Compliance, Research Participant Safety, Chemotherapy, Radiation Therapy, Leadership, Recruitment, Accrual, Documentation, IATA Guidelines, Healthcare Team Interaction, Clinical Trials

Industry

Hospitals and Health Care

Description

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. Education Bachelors Degree (Required) Graduate Level Classes or Degree in a relevant program (Preferred) Combination of relevant education and experience may be considered in lieu of degree. Experience 2 Years experience in a healthcare setting preferably oncology or clinical trials. (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) License/Certifications CCRC - Cert Clin Research Coordinator (Preferred) CCRP - Cert Clin Research Prof (Preferred) CCRA - Cert Clin Research Associate (Preferred) _

Responsibilities

This position coordinates and facilitates the conduct of clinical research protocols, ensuring participant recruitment, protocol compliance, and data quality. The role also involves interaction with investigators, healthcare team members, and research participants to support clinical trials.