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Pay range for this position is $36.68 - $54.40/hour. Actual pay is based on years of licensure. This is a Salaried position.
Overview
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).
Qualifications
REQUIRED QUALIFICATIONS:
Education:
Bachelor of Science in Nursing
Licenses/Certifications:
RN-Registered Nurse BLS From the American Heart Association
Experience:
3 years of experience as a RN Clinical Research Coordinator
Other skills/knowledge:
- 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.
PREFERRED QUALIFICATIONS:
Education:
Master’s or other advanced degree in clinical research, nursing, healthcare, business or related field
License/Certifications:
Certified Clinical Research Coordinator or Professional (CCRC or CCRP)
Experience:
- 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.
OSF HealthCare is an Equal Opportunity Employer.