CLINICAL RESEARCH COORD II at Temple University Health System

Philadelphia, Pennsylvania, United States -

Full Time

Start Date

Immediate

Expiry Date

09 Jun, 26

Salary

0.0

Posted On

11 Mar, 26

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

Skills

Clinical Research, Protocol Compliance, Participant Recruitment, Data Quality, Trial Monitoring, Study Activation, Protocol Amendments, Oncology, Chemotherapy, Radiation Therapy, Phlebotomy, Specimen Processing, CCRC, CCRP, ACRP-CP

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. CCRC, CCRP or ACRP-CP certification is required within 1 year from date of hire. Education Bachelor's Degree Required Master's Degree Preferred or Combination of relevant education and experience may be considered in lieu of degree Required Experience 2 years experience in a Clinical Research Coordinator role or 5 Years experience in related clinical research role Required 2 years experience with oncology clinical trials Preferred 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 Required or Cert Clin Research Prof Required or Assn Clin Res Prof - Cert Prof Required

Responsibilities

Coordinates and facilitates clinical research protocols, ensuring participant recruitment, safety, and data quality. This role involves developing monitoring tools, managing trial accrual, and coordinating study activation and amendments.