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.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
Bachelors Degree (Required)
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)License/Certifications
RN-LIC - PA Registered Nurse License (Required)
ONCC - Oncology Nursing Cert Corp (Preferred)
CCRP - Cert Clin Research Prof (Preferred)