RN Coordinator, Clinical Research Oncology
About The Position
Exciting opportunity to join OSF HealthCare's Early Phase Oncology Research Program and collaborate with an interdisciplinary team on groundbreaking studies advancing cancer detection and treatment. This role offers the chance to contribute to innovations shaping the future of oncology care. POSITION SUMMARY: The Coordinator Clinical Research RN II (CRC RN II) is a specialized research professional working with, and under the direction of the Principal Investigator (PI). While the PI is primarily responsible for the overall design, conduct, and management of the research studies, the RN CRC II supports, facilitates and coordinates the daily clinical research activities and plays a critical role in the conduct of the research at the institution. The CRC RN II must exhibit a moderate level of expertise in the conduct of clinical research and will complete most research tasks independently with minimal direction. The CRC RN II in collaboration with the PI is responsible for assuring research is conducted in an ethical manner and all study activities are completed by strictly following Good Clinical Practices (GCP). The CRC RN II is responsible for both clinical and administrative business functions relating to their assigned projects and play a critical liaison role between study team, department leadership, Institution, Sponsors, and Institutional Review Board (IRB).
Requirements
- Bachelor of Science in Nursing
- RN-Registered Nurse
- BLS From the American Heart Association
- 3 years of experience as a RN Clinical Research Coordinator
- Excellent interpersonal and communication skills.
- Solid computer skills, including proficiency with Microsoft software.
- Strong analytical and problem solving skills, with the ability to be detail oriented.
Nice To Haves
- Master's or other advanced degree in clinical research, nursing, healthcare, business or related field
- Certified Clinical Research Coordinator or Professional (CCRC or CCRP)
- Oncology Phase 1 - Phase IV clinical trial experience
- Strong Project Management Skills
- Understanding of research regulations (e.g. IRB, FDA, OHRP, GCP, etc.)
- Experience with electronic health records and data capturing systems.
Benefits
- comprehensive and market-competitive total rewards package that includes benefits, compensation, recognition and well-being offerings that focus on the whole person and engage with their current stage of life and career.
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What This Job Offers
Job Type
Full-time
Career Level
Mid Level
Industry
Religious, Grantmaking, Civic, Professional, and Similar Organizations
Number of Employees
1-10 employees
