Coordinator-Research Nurse II RN

Baptist; Memphis (TN); On-site; USD 60,000 - 75,000; Full time

Job summary

Baptist Health Memphis seeks a Research Coordinator, RN-II to coordinate clinical trials and ensure adherence to Good Clinical Practice, sponsor regulations, and internal policies. The role includes patient care, recruitment, screening, enrollment, data submission, and follow-up, with collaboration across study teams and regulatory staff.

The position requires a current RN license and a Bachelor’s degree in Nursing, plus 4 years of oncology or clinical research experience; BLS within 14 days of

Qualifications

• RN license and Bachelor's in Nursing required.
• 4 years of research or clinical research experience.
• 4 years’ experience in Oncology and/or Clinical Research.
• BLS within 14 days of hire.
• Certifications: SOCRA, ACRP, CITI, HAZMAT, CCRP or CCRC.

Responsibilities

• Facilitates compliance with research protocol and good clinical practice.
• Communicates with research team to facilitate clinical trials.
• Demonstrates leadership in informed consent discussions.
• Manages activities of patients in clinical trials.
• Ensures collection of source data and documentation integrity.
• Enhances recruitment and ethical practices in trials.

Skills

Leadership

Communication

Education

Bachelor’s Degree in Nursing

RN License

Tools

SOCRA Certification

ACRP Certification

CITI Certification

HAZMAT Certification

CCRP/CCRC

Job description

The research coordinator, RN- II is responsible for coordinating the conduct of research protocols under general supervision, assuring that 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 guidelines, BMHCC and BCRI policies and procedures. The nurse research coordinator II is responsible for patient clinical care and management, recruitment, screening, scheduling, enrollment, submission of data, randomization and patient follow-up. The nurse research coordinator II is also responsible for specific protocol implementation and management. The research coordinator, RN- II may act as a liaison between the hospital, the IRB, study sponsors, and all investigators. The research coordinator, RN- II will collaborate with research coordinators, data managers and regulatory specialists. Travel may be required.

Responsibilities

• Facilitates compliance with the requirements of the research protocol and good clinical practice while remaining cognizant of the needs of diverse patient populations.
• Communicates with research team to facilitate the effective conduct of clinical trials.
• Demonstrates leadership in ensuring patient comprehension and safety during initial and ongoing clinical trial informed consent discussions.
• Manages the activities of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, and reporting requirements.
• Ensures collection of source data and completion of documentation that validate the integrity of the conduct of the clinical trial
• Enhances recruitment while being mindful of the needs of diverse patient populations.
• Assists in implementation of recruitment plans to identify and assess individuals who might be eligible for clinical trials, taking into consideration the study entry criteria, required procedures, and other potential factors.
• Enhances adherence to ethical practices during the conduct of clinical trials in order to protect the rights and well-being of patients and the collection of quality data.
• Identifies financial variables that affect research and supports good financial stewardship in clinical trials.
• Identifies his or her ongoing professional development needs and seeks resources and opportunities to meet those needs, such as memberships in nursing, oncology, or research organizations.
• Other duties as assigned.

Specifications

Experience

• 4 years Research or Clinical Research Experience
• 4 Years’ Experience in Oncology and/or Clinical Research

Education

• Currently licensed nurse or equivalent combination of education and experience
• Bachelor’s Degree in Nursing

Licensure

• RN License
• BLS within 14 days of hire,
• Certifications- SOCRA (Society of Clinical Research Associates), ACRP (Association of Clinical Research Professionals), Collaborative Institutional Training Initiative (CITI), HAZMAT, CCRP or CCRC