What are the responsibilities and job description for the RN- Clincial Trials position at Baton Rouge General?
Be part of a mission-driven team advancing healthcare through research and innovation. This role offers the opportunity to make a direct impact on patient outcomes while working in a collaborative and supportive environment.
We are seeking a dedicated and detail-oriented Registered Nurse (RN) to support clinical research activities through effective protocol management and patient-centered care. This role is responsible for implementing clinical study requirements, coordinating research activities, and ensuring the safety, rights, and well-being of study participants. The RN will also provide operational and administrative support related to clinical trials while delivering care aligned with the nursing process: assessment, planning, implementation, and evaluation.
Key Responsibilities
Clinical Protocol Management
- Participate in planning and implementation of clinical research protocols
- Screen patients for eligibility and review diagnostic results
- Educate patients and guide them through the informed consent process
- Enroll eligible participants into clinical trials
- Coordinate study-related appointments, treatments, and follow-ups
- Ensure accurate data collection, processing, and documentation per protocol
- Monitor and report adverse events, protocol deviations, and study outcomes
- Maintain complete and compliant source documentation
Regulatory Oversight
- Ensure timely submission of regulatory documents to sponsors and review boards
- Maintain compliance with Institutional Review Board (IRB) and organizational policies
- Uphold all legal, ethical, and regulatory standards in research conduct
Collaboration & Problem Solving
- Educate and support hospital staff on study-specific procedures
- Communicate effectively with internal teams, sponsors, and stakeholders
- Apply critical thinking to resolve clinical and operational challenges
- Active Louisiana RN License
- Minimum of 3 years of clinical trials experience
- Strong understanding of clinical research principles and regulatory requirements
- Proficiency with computers and research-related software systems
- Excellent organizational, communication, and coordination skills
- Ability to manage multiple priorities in a fast-paced environment