EXTRAMURAL CLIN RESEARCH COORD at Temple University Health System

Philadelphia, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

10 Jun, 26

Salary

0.0

Posted On

12 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research Protocol Coordination, Specimen Handling, IATA Guidelines Compliance, Research Participant Recruitment, Protocol Compliance, Research Participant Safety, Data Quality Management, Data Management, Investigator Interaction, Healthcare Team Coordination, Clinical Trial Conduct, Phlebotomy, Specimen Processing, Chemotherapy Knowledge, Radiation Therapy Knowledge

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 Bachelor's Degree Required 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 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 Licenses Cert Clin Research Coordinator Preferred Cert Clin Research Prof Preferred Cert Clin Research Associate Preferred

Responsibilities

This role coordinates and facilitates clinical research protocols, including specimen collection, documentation, and shipment according to IATA guidelines. The coordinator also provides leadership to ensure participant recruitment, protocol compliance, safety, and data quality across various campuses.