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Coordinator-Research Nurse I RN

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. Baptist Memorial Health Care is hiring for its own floors, with no agency in between.

Posted Sep 22 · 2 years of experience

Shift and hours
Rotating
Unit and setting
Hospital
License
RN license BLS certification within 14 days; RN License required by state.RN License required by state

Do you qualify?

License
RN License required by state BLS certification within 14 days; RN License required by state.
Experience
2 years of research or clinical experience 2 years of Research or Clinical experience
Also asks
currently licensed nurse or equivalent combination of education and experience Currently licensed nurse or equivalent combination of education and experience

Preferred

Certification
SOCRA, ACRP, CITI, HAZMAT, CCRP or CCRC certifications
Education
Bachelor's degree in Nursing Preferred/Desired bachelors degree in Nursing.
Experience
2 years of oncology or clinical research experience 2 years of Oncology or Clinical Research Experience
Also asks
computer skills including MS Word, organizational skills, detail oriented, and EMR/CTMS experience

The role and schedule

Day to day
facilitate compliance with research protocol and good clinical practice Facilitates compliance with the requirements of the research protocol and good clinical practice while remaining cognizant of the needs of diverse patient populations.
Day to day
communicate with research team to facilitate clinical trials Communicates with research team to facilitate the effective conduct of clinical trials.
Day to day
ensure patient comprehension and safety during informed consent discussions Demonstrates leadership in ensuring patient comprehension and safety during initial and ongoing clinical trial informed consent discussions.
Day to day
manage clinical trial patient activities and protocol compliance Manages the activities of patients participating in clinical trials, ensuring compliance with protocol procedures, assessments, and reporting requirements.
Day to day
collect source data and complete documentation Ensures collection of source data and completion of documentation that validate the integrity of the conduct of the clinical trial.
Day to day
enhance patient recruitment mindful of diverse populations Enhances recruitment while being mindful of the needs of diverse patient populations.
Day to day
enhance adherence to ethical practices during clinical trials 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.
Day to day
identify financial variables and support good financial stewardship Identifies financial variables that affect research and supports good financial stewardship in clinical trials.
Day to day
pursue professional development needs and professional memberships
Charting
EMR and Clinical Trial Management System Experience with EMR and Clinical Trial Management System
Travel
travel may be required Travel may be required.

Your fit

Questions to ask

  • Can you walk me through base pay range and differentials?
  • What should I expect for weekly hours, weekend, holiday, call, and rotation?
  • What orientation, preceptor time, and ongoing unit support are included?
  • How are patient load, floating, and staffing support handled day to day?
Build questions for this role

Original listing

Read full text

Overview

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.

Special Skills

Preferred/Desired

  • 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

What's around it?

In Memphis, TN

Memphis, TNFrom Census ACS 2024.

Living costs about 8% below the US average

Median rent
$1,181/mo
Household income
$51,736/yr, all local households, not nurse pay

See Memphis, TN

Nurses on this role

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