Coordinator-Research Nurse I RN

Baptist • Southaven, MS

7d

About The Position

The Research Coordinator, RN-I coordinates research protocols and ensures the integrity and quality of research in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations and guidelines, and BMHCC and BCRI policies and procedures. The role coordinates clinical research activities and patient clinical care and management, including recruitment, screening, scheduling, enrollment, data submission, randomization, and patient follow-up. The position may serve as a liaison among the hospital, IRB, study sponsors, and investigators, and collaborates with research coordinators, data managers, and regulatory specialists. Travel may be required.

Requirements

• At least 2 years of research or clinical experience.
• Currently licensed nurse, or an equivalent combination of education and experience.
• BLS certification within 14 days.
• RN license required by the state.

Nice To Haves

• 2 years of oncology or clinical research experience.
• Bachelor's degree in Nursing.
• Computer skills, including MS Word.
• Excellent organizational skills.
• Detail-oriented.
• Experience with an EMR and Clinical Trial Management System.
• Certifications such as SOCRA, ACRP, CITI, HAZMAT, CCRP, or CCRC.

Responsibilities

• Facilitate compliance with research protocol and Good Clinical Practice requirements while considering the needs of diverse patient populations.
• Communicate with the research team to facilitate effective conduct of clinical trials.
• Promote patient comprehension and safety during initial and ongoing clinical trial informed consent discussions.
• Manage activities of clinical trial patients, ensuring compliance with protocol procedures, assessments, and reporting requirements.
• Ensure collection of source data and completion of documentation that validates the integrity of clinical trial conduct.
• Enhance recruitment while considering the needs of diverse patient populations.
• Promote ethical practices in clinical trials to protect patient rights and well-being and support the collection of quality data.
• Identify financial variables affecting research and support good financial stewardship in clinical trials.
• Identify ongoing professional development needs and seek resources and opportunities to address them.
• Perform other responsibilities as assigned.

What This Job Offers

• Job Type: Full-time
• Career Level: Entry Level
• Education Level: No Education Listed