Coordinator-Research Nurse I RN

Baptist Memorial Health Care; Memphis (TN); On-site; USD 48,000 - 95,000; Full time

Job summary

An established industry player is seeking a dedicated Research Coordinator, RN-I to oversee the execution of clinical research protocols. This role is pivotal in maintaining the integrity and quality of research while adhering to Good Clinical Practice Guidelines. You will collaborate closely with various stakeholders, including patients, investigators, and regulatory bodies, ensuring a seamless flow of information and adherence to ethical standards. If you are passionate about clinical research and patient care, this position offers an exciting opportunity to make a significant impact in the healthcare field.

Qualifications

• Minimum 2 years of research or clinical experience required.
• Preferred 2 years of oncology or clinical research experience.

Responsibilities

• Coordinate clinical research activities and ensure compliance with protocols.
• Manage patient participation and ensure safety during clinical trials.

Skills

Clinical Research

Patient Management

Good Clinical Practice

Data Collection

Patient Recruitment

Communication Skills

Organizational Skills

Education

RN License

Bachelor's Degree in Nursing

Tools

EMR Systems

Clinical Trial Management System

MS Word

Job description

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Join to apply for the Coordinator-Research Nurse I RN role at Baptist Memorial Health Care

Job Summary

The Research Coordinator, RN- I is responsible for coordinating the conduct of research protocols, 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. This includes the coordination of clinical research activities, patient clinical care and management, recruitment, screening, scheduling, enrollment, submission of data, randomization and patient follow-up. This position may act as a liaison between the hospital, the IRB, study sponsors, and all investigators. This position will collaborate with research coordinators, data managers and regulatory specialists. Travel may be required.

Overview

Job Summary

The Research Coordinator, RN- I is responsible for coordinating the conduct of research protocols, 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. This includes the coordination of clinical research activities, patient clinical care and management, recruitment, screening, scheduling, enrollment, submission of data, randomization and patient follow-up. This position may act as a liaison between the hospital, the IRB, study sponsors, and all investigators. This position 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.
• 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 responsibilities as assigned.
  
  

Specifications

Experience

Minimum Required

• 2 years of Research or Clinical experience
  
  

Preferred/Desired

• 2 years of Oncology or Clinical Research Experience
  
  

Education

Minimum Required

• Currently licensed nurse or equivalent combination of education and experience
  
  

Preferred/Desired

• Preferred/Desired bachelors degree in Nursing.
  
  

Training

Preferred/Desired

Minimum Required

Preferred/Desired

Special Skills

• Computer skills to include MS Word, Excellent organizational skills. Detail oriented. Experience with EMR and Clinical Trial Management System
  
  

Licensure

Minimum Required

• BLS certification within 14 days; RN License required by state.
  
  

Preferred/Desired

• Certifications - SOCRA (Society of Clinical Research Associates), ACRP (Association of Clinical Research Professionals), Collaborative Institutional Training Initiative (CITI), HAZMAT, CCRP or CCRC

Seniority level

• Seniority level

  Entry level

Employment type

• Employment type

  Other

Job function

• Job function

  Health Care Provider

• Industries

  Hospitals and Health Care

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