Coordinator-Research Nurse RN

Job Summary

The Research Coordinator, RN‑I is responsible for coordinating the conduct of research protocols, assuring the integrity and quality of the research is maintained, and that the research is conducted in accordance with Good Clinical Practice Guidelines, federal and sponsor regulations, and BMHCC and BCRI policies and procedures. This includes coordinating clinical research activities, patient clinical care and management, recruitment, screening, scheduling, enrollment, data submission, randomization, and patient follow‑up.

The position may act as a liaison between the hospital, the IRB, study sponsors, and all investigators, collaborating with research coordinators, data managers, and regulatory specialists. Travel may be required.

• Facilitate compliance with the research protocol and good clinical practice while remaining cognizant of the needs of diverse patient populations.
• Communicate with the research team to facilitate the effective conduct of clinical trials.
• Demonstrate leadership in ensuring patient comprehension and safety during initial and ongoing clinical trial informed consent discussions.
• Manage the activities of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, and reporting requirements.
• Ensure collection of source data and completion of documentation that validate the integrity of the conduct of the clinical trial.
• Enhance recruitment while being mindful of the needs of diverse patient populations.
• Enhance adherence to ethical practices during the conduct of clinical trials to protect the rights and well‑being of patients and the collection of quality data.
• Identify financial variables that affect research and support good financial stewardship in clinical trials.
• Identify ongoing professional development needs and seek resources and opportunities to meet those needs, such as memberships in nursing, oncology, or research organizations.
• Other responsibilities as assigned.

• Minimum
  
  Required:
  
  2 years of Research or Clinical experience.
• Preferred/Desired: 2 years of Oncology or Clinical Research Experience.

• Minimum
  
  Required:
  
  Currently licensed nurse or equivalent combination of education and experience.
• Preferred/Desired:
  Bachelor’s degree in Nursing.

• Computer skills including MS Word, excellent organizational skills, detail oriented, experience with EMR and Clinical Trial Management System.

• Minimum
  
  Required:
  
  BLS certification within 14 days; RN license required by state.
• Preferred/Desired:
  Certifications – SOCRA, ACRP, CITI, HAZMAT, CCRP or CCRC.