Clinical Research Nurse Coordinator - Oncology Trials
Overview
This role owns clinical trial coordination and patient care for oncology studies at UKH, ensuring protocol compliance and patient safety. You will collaborate with investigators, sponsors, and nursing staff to prepare and execute trials, balancing research demands with patient needs. The position offers a chance to apply RN expertise in a research-focused setting while contributing to quality improvement and education. You will work onsite in Kansas City, supporting a part-time schedule.
What You'll Do9
- 1Prepare for upcoming clinical trials by reviewing protocols with investigators, coordinators, and sponsors.
- 2Perform study tasks per GCP and protocol, including administering investigational drugs and devices.
- 3Educate patients and staff on trial procedures, investigational products, and safety protocols.
- 4Maintain subject safety and confidentiality, implementing HIPAA and legal protections.
- 5Document patient data in EMR with accuracy and timeliness for research reporting.
- 6Coordinate care continuity across admissions, discharges, and ER visits.
- 7Identify quality improvement opportunities and implement action plans with the team.
- 8Administer medications safely and monitor reactions per protocol.
- 9Support IRB and FDA communication as needed for study compliance.
Requirements9
- 1Bachelor Degree in Nursing or higher
- 22+ years of clinical RN experience
- 3Licensed Registered Nurse (multi-state) and BLS certification
- 4Training in Human Subjects Protection, GCP, HIPAA, and informed consent
- 5IV therapy skills
- 6Basic typing and word processing ability
- 7Analytical, critical thinking, and problem-solving skills
- 8Knowledge of clinical trial development and regulatory processes preferred
- 9Chemo certification preferred
Salary Insight
Salary not disclosed in listing
Location
Required Skills
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