Medix
Clinical Research Nurse (Oncology)
Location:
Nashville, TN Schedule:
MondayFriday, 8:00 AM5:00 PM
Overview Join one of the nations leading academic medical centers as a Clinical Research Nurse! In this role, youll support groundbreaking oncology research while focusing on patient care. Under the supervision of the Principal Investigator, youll ensure the integrity and quality of clinical trials, from recruitment through completion, in compliance with Good Clinical Practice (GCP) guidelines, federal regulations, and policies.
This position offers the opportunity to be deeply involved in innovative cancer research while maintaining a meaningful connection with patients!
Key Responsibilities Recruit, screen, and enroll study participants; ensure compliance with study protocols. Coordinate all aspects of clinical trials, including scheduling, documentation, and follow-up. Conduct study-related procedures per protocol (lab draws, specimen collection, medication handling, etc.). Maintain accurate, timely study records and regulatory documentation (IRB submissions, adverse event reports). Serve as a liaison between investigators, sponsors, participants, and internal teams. Identify and resolve issues to ensure participant safety and data accuracy. Participate in site visits, audits, and ongoing quality improvement initiatives. Educate participants and staff on study procedures and informed consent.
Qualifications Required: Active RN license
(State of TN or compact state) 3+ years of nursing experience Minimum 1 year of oncology experience
(hospital, clinic, or research setting) Strong organizational and communication skills Preferred: Prior
clinical research nursing
experience (oncology focus ideal) Working knowledge of
FDA, OHRP, GCP/ICH, and HIPAA
regulations Soft Skills Detail-oriented and able to multitask across multiple studies Strong critical thinking and problem-solving abilities Compassionate patient care approach Collaborative, positive attitude with a focus on team success
Nashville, TN Schedule:
MondayFriday, 8:00 AM5:00 PM
Overview Join one of the nations leading academic medical centers as a Clinical Research Nurse! In this role, youll support groundbreaking oncology research while focusing on patient care. Under the supervision of the Principal Investigator, youll ensure the integrity and quality of clinical trials, from recruitment through completion, in compliance with Good Clinical Practice (GCP) guidelines, federal regulations, and policies.
This position offers the opportunity to be deeply involved in innovative cancer research while maintaining a meaningful connection with patients!
Key Responsibilities Recruit, screen, and enroll study participants; ensure compliance with study protocols. Coordinate all aspects of clinical trials, including scheduling, documentation, and follow-up. Conduct study-related procedures per protocol (lab draws, specimen collection, medication handling, etc.). Maintain accurate, timely study records and regulatory documentation (IRB submissions, adverse event reports). Serve as a liaison between investigators, sponsors, participants, and internal teams. Identify and resolve issues to ensure participant safety and data accuracy. Participate in site visits, audits, and ongoing quality improvement initiatives. Educate participants and staff on study procedures and informed consent.
Qualifications Required: Active RN license
(State of TN or compact state) 3+ years of nursing experience Minimum 1 year of oncology experience
(hospital, clinic, or research setting) Strong organizational and communication skills Preferred: Prior
clinical research nursing
experience (oncology focus ideal) Working knowledge of
FDA, OHRP, GCP/ICH, and HIPAA
regulations Soft Skills Detail-oriented and able to multitask across multiple studies Strong critical thinking and problem-solving abilities Compassionate patient care approach Collaborative, positive attitude with a focus on team success