Supervisor of Clinical Research

Location

Stockton, CA | United States

Job description

As one of the nation's largest nonprofit systems, CommonSpirit Health has over 2,200 care sites and 140 hospitals in 24 states. We serve some of the most diverse communities across the nation, and in each location, humankindness leads the way. 

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.

While you're busy impacting the healthcare industry, we'll take care of you with benefits that include:
Medical/Dental/Vision, FSA, Dependent Care Spending Account, Life Insurance, Short and Long-term Disability, 401k match, Paid Time Off, Wellness Program, Tuition Reimbursement, Accidental Insurance, Critical Illness Insurance, Identity Theft Protection, Employee Assistance Program, and more!

Reporting to the Division Research Manager the Clinical Research Site Supervisor is responsible for overseeing the coordination and management of multiple clinical trials and research projects at St. Joseph’s Medical Center in Stockton, CA, a facility of the CommonSpirit Health Research Institute (CSHRI). This position will supervise an on-site team of RN and non-RN research coordination staff who support Principal Investigators, co- and sub-investigators, clinical and ancillary departments, IRBs, and industry or government sponsors. The primary focus of this research site is management of prospective oncology and cardiovascular drug and device clinical trials. The Site Supervisor will be accountable for providing staff training, project leadership, and quality control oversight for clinical research coordinators and/or clinical research nurses. This position will: 

• Plan, coordinate, implement, and complete clinical trials and research projects,
• Provide support to the research coordination team
• Assist in the care and assessment of research participants, ensuring compliance with all applicable federal and state regulations, as well as CommonSpirit Health policy.

• Bachelor’s degree, in a science or health related field, required
• Demonstrated leadership competencies in the management of others required.
• Minimum one year full time experience in role performing duties as a Senior Research Coordinator
• Minimum 7 years of progressively responsible experience coordinating clinical trials required; worked as primary research coordinator for at least 20 drug or device trials
• Experience supporting and managing prospective oncology, cardiovascular and neuroscience drug and device clinical trials strongly preferred
• Minimum of 7 years of experience interacting with patients in a healthcare setting required
• Experience in preparing and maintaining regulatory documents and other IRB related study documentation required
• SOCRA or ACRP certification required or must meet eligibility criteria for certification within one year of hire

#LI-CSH

Job tags

Salary