CLINICAL RESEARCH NURSE II

Temple University Health System • Philadelphia, PA

1h • Hybrid

About The Position

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.

Requirements

• Bachelor's Degree Required
• 2 years experience as a Clinical Research Nurse Required
• 2 years experience in nursing with a focus on oncology or comparable clinical environment Required
• 2 years experience with oncology or equivalent clinical trials Required
• PA Registered Nurse License Required
• Multi State Compact RN License Required

Nice To Haves

• Master's Degree Preferred
• General Experience and knowledge of chemotherapy administration and/or radiation therapy treatment modalities Preferred
• 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.
• 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.
• Work closely with the members of the clinical research team to develop effective tools for close monitor and reporting of trials accrual.
• Coordinate the timely study activation and submission of protocol amendments.
• Interact with institutional investigators, other members of healthcare team, service line members and research participants/families in a manner, which supports the conduct of clinical trials.

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level