CLINICAL RESEARCH NURSE at Temple Health System
Philadelphia, Pennsylvania, United States -
Full Time


Start Date

Immediate

Expiry Date

12 Mar, 26

Salary

0.0

Posted On

12 Dec, 25

Experience

2 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Clinical Research, Protocol Compliance, Participant Recruitment, Data Quality, Oncology Nursing, Chemotherapy Administration, Study Activation, Protocol Amendments, Leadership, Team Collaboration, Patient Safety, Monitoring, Reporting, Healthcare Interaction, Research Coordination, Trial Management

Industry

Hospitals and Health Care

Description
Coordinate and facilitate the conduct of clinical research protocols which may be supported by NCI, industry, cooperative groups, or grant funded and investigator-initiated. Provide 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 monitor 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 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 Other Graduate Level Classes or Degree in a relevant program Preferred Experience 2 years experience as a Clinical Research Nurse Preferred 2 years experience in nursing with a focus on oncology Preferred 2 years experience with oncology clinical trials Preferred General Experience and knowledge of chemotherapy administration Preferred Licenses PA Registered Nurse License Required Oncology Nursing Cert Corp Preferred Cert Clin Research Prof Preferred or Cert Clin Research Coordinator Preferred or Cert Clin Research Associate Preferred
Responsibilities
Coordinate and facilitate the conduct of clinical research protocols, ensuring participant recruitment, protocol compliance, and data quality. Work closely with the clinical research team to develop tools for monitoring trials and coordinate study activation.
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