Coordinator-Research Nurse I RN

Baptist•Southaven, MS

17h

About The Position

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 Minimum Required Preferred/Desired Special Skills Minimum Required 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

Requirements

2 years of Research or Clinical experience
Currently licensed nurse or equivalent combination of education and experience
Computer skills to include MS Word
Excellent organizational skills.
Detail oriented.
Experience with EMR and Clinical Trial Management System
BLS certification within 14 days
RN License required by state.

Nice To Haves

2 years of Oncology or Clinical Research Experience
Preferred/Desired bachelors degree in Nursing.
Certifications - SOCRA (Society of Clinical Research Associates), ACRP (Association of Clinical Research Professionals), Collaborative Institutional Training Initiative (CITI), HAZMAT, CCRP or CCRC

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.