RN- Clincial Trials

Description

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

Requirements

• 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