Clinical Research Nurse II: Study Coordinator

University of Louisville; South Dakota; On-site; USD 69,000 - 103,000; Full time

Job summary

The University of Louisville is seeking a Clinical Research Nurse II to coordinate clinical trials across Oncology/Hematology, Radiation Oncology and Bone Marrow Transplant. The CRN ensures protocol compliance, patient safety and data integrity, acting as a liaison among investigators, sponsors and staff.

Ideal candidates hold a Bachelor’s in Nursing with a Kentucky license and have 2+ years of related experience; ACRP, SoCRA or OCN certification is preferred.

Qualifications

• Bachelor’s degree in Nursing with current Kentucky license and two years of related research or nursing experience.
• ACRP or SoCRA certification preferred (OCN)

Responsibilities

• Coordinates all aspects of clinical trials initiation to ensure full compliance with sponsors and FDA.
• Plan recruitment methods and screen patients for eligibility; educate patients and families about trials.
• Coordinate logistics of patient visits and testing required by protocol; liaise between investigators, sponsors and staff.
• Ensure accurate data collection, source documents and regulatory submissions as required.
• Maintain protocol training and certifications; assist in staff education on new studies and requirements.

Skills

ACRP certification

SoCRA certification

Education

Bachelor’s degree in Nursing; Kentucky license

Job description

The University of Louisville is seeking a Clinical Research Nurse II to coordinate clinical trials across Oncology/Hematology, Radiation Oncology and Bone Marrow Transplant. The CRN ensures protocol compliance, patient safety and data integrity, acting as a liaison among investigators, sponsors and staff.

Ideal candidates hold a Bachelor’s in Nursing with a Kentucky license and have 2+ years of related experience; ACRP, SoCRA or OCN certification is preferred.