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Clinical Research Oncology RN Supervisor - San Luis Obispo, United States - CommonSpirit Health
Description
Overview
As one of the nation's largest nonprofit systems, CommonSpirit Health has over 2,200 care sites and 140 hospitals in 24 states.
The CommonSpirit Health Research Institute offers comprehensive clinical research services and support for various research activities.
Their primary focus includes multi-site clinical trials, local and large-scale data research, partnerships with industry and academia for technology and innovation research, physician-initiated research, resident-initiated research in teaching facilities, nurse-initiated research, and health sciences student-initiated research.
The institute aims to provide start-to-finish research services and assist in advancing medical knowledge and patient care.This position will cover facilities supporting oncology studies in San Luis Obispo, CA, and surrounding areas.
We will consider candidates who would need to relocate with relocation assistance offered.
Responsibilities
The Clinical Research Site Supervisor-RN (Oncology) oversees a team of research coordination staff who support Principal Investigators and other departments involved in clinical trials and research projects managed by the CommonSpirit Health Research Institute (CSHRI).
The primary responsibilities of this role include:
Managing all aspects of multiple clinical trials or research projects
Ensuring compliance with regulations and CSH policies
Providing staff training and project leadership
Maintaining quality standards.
Qualifications
A bachelor's degree in a science or health-related field required
Current RN license in state of employment and BLS certification required
Minimum five years of experience coordinating oncology clinical trials
Certification (CCRP or CCRC) by SOCRA or ACRP is required
Certificate of Human Subjects Protection and Good Clinical Practice training required
Minimum one year of experience as a Senior Research Coordinator
Demonstrated leadership competencies in the management of others required
Minimum one year full time experience supervising research personnel strongly preferred
Experience interacting with patients in a healthcare setting is required
Experience in implementing research protocols and clinical trial processes required
Experience in preparing and maintaining regulatory documents and IRB-related study documentation required
Competencies in training staff and investigators on clinical trial processes required
Thorough knowledge of research regulatory requirements, including FDA, OHRP, and GCP, required
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Pay Range
$ $72.00 /hour
We are an equal opportunity/affirmative action employer.