CLINICAL RESEARCH COORD at Temple University Health System

Philadelphia, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

19 Jul, 26

Salary

0.0

Posted On

20 Apr, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical research coordination, Protocol compliance, Participant recruitment, Data quality management, Study activation, Protocol amendments, Oncology, Clinical trials, Phlebotomy, Specimen processing, Chemotherapy administration, Radiation therapy administration, Regulatory reporting

Industry

Hospitals and Health Care

Description

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. 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 direct experience in a healthcare setting preferably oncology or clinical trials or a minimum of 3 Years related experience Required General Experience and knowledge of chemotherapy and/or radiation therapy administration Preferred General Experience Previous experience performing phlebotomy and specimen processing Preferred Licenses Cert Clin Research Coordinator Preferred or Cert Clin Research Prof Preferred or Assn Clin Res Prof - Cert Prof Preferred

Responsibilities

Coordinates and facilitates clinical research protocols to ensure participant safety, protocol compliance, and high data quality. Collaborates with the clinical research team to manage trial accrual, study activation, and the submission of protocol amendments.