Clinical Research Coordinator II

The Clinical Research Coordinator II (CRC-II) is responsible for the coordination of all day-to-day clinical research activities with minimal supervision. The CRC-II is assigned more complex studies, including but not limited to Phase II and Phase III therapeutic clinical trials for various types or stages of cancer. The CRC-II is responsible for coordinating multiple clinical trials simultaneously and ensures full compliance with each research protocol adhering to applicable federal regulations, Good Clinical Practice (GCP), SJ/C Policies & Procedures, and Institutional Review Board (IRB) requirements. The CRC-II works with clinical investigators to recruit diverse research participants representative of the site’s catchment area. Key tasks of the CRC-II include but are not limited to the following: obtains informed consent, confirms participant eligibility, coordinates participant schedules to comply with research protocol requirements, and ensures the participant’s overall care is coordinated per the parameters set forth in the research protocol. The CRC-II also collects and processes blood or other biospecimens, performs EKGs or other clinical assessments as required by the research study, and collects & reports participant data. Responsibilities

Adherence to Ethical Standards: Promotes ongoing compliance with the key ethical concepts of research, including respect for individuals, beneficence, and justice. Protocol Compliance: Communicates with the interdisciplinary team to ensure protocol compliance and timeliness of protocol-related procedures. Informed Consent: Ensures that the most current version of the IRB approved protocol consent document and HIPAA authorization document is used when consenting a patient. Participant Recruitment & Retention: Identify, screen and enroll participants to clinical trials per established goals. Management of Clinical Trial Participants: Educates the patient and family regarding clinical trial participation, clinical condition, and/or disease process. Documentation and Document Management: Documents all participant encounters in the medical record and/or research record. Data Management: Adheres to study requirements for reporting research data. Requirements

Associate's in Healthcare or Social Sciences - Required Bachelor's of Science in Nursing - Preferred 1-2 Years Clinical Research experience or 3 Years Nursing experience - Required 2-3 Years Oncology experience - Preferred Nurse candidates: Professional License with State of Practice - Required CCRC, CCRP, or OCN certification required within 18 months of hire or upon eligibility. Basic Life Support (BLS) - Required

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