Clinical Research Supervisor
UC Irvine
Your Role on the Team The Clinical Research Supervisor 1 will manage day-to-day research operations and provide comprehensive oversight for clinical research activities within the Department of Radiology. The incumbent will coordinate and manage clinical research studies and sponsored clinical trials, ensuring adherence to Good Clinical Practices (GCP), internal SOPs, and university policies. Responsibilities include reviewing study protocols, ensuring regulatory compliance, facilitating communication among research staff, principal investigators, sponsors and regulatory offices, supporting clinical research faculty and staff, curating data, planning experiments, coordinating radiology safety reviews, and performing root‑cause analysis to maintain smooth workflow. Requirements Broad knowledge of clinical research concepts, federal, state and local laws and regulations, and industry requirements. Broad theoretical and operational knowledge of clinical and patient safety standards and regulations. Ability to think critically in compiling and reviewing data from various sources. Ability to perform scientific research including evaluating information and preparing concise, well‑organized reports and correspondence. Database creation and maintenance using Excel and other relational databases. Research experience with IRB, IACUC, HIPAA, GCP, and ethical conduct of research. Excellent verbal and written communication skills and ability to interact with the public, faculty, and staff. Ability to establish and maintain files and records. High level of integrity and honesty in maintaining confidentiality. Ability to quickly evaluate complex issues and identify options for resolution. Ability to work collaboratively with cross‑functional teams. Bachelor’s degree in a related area and/or equivalent experience/training. 7+ years of related work experience. Preferred Experience in clinical coordination. Familiarity with UC system policies and procedures. Experience with EPIC, Redcap, OnCore, and Kuali Financial System. Advanced degree preferred. Certified Clinical Research Professional (CCRP). Total Rewards In addition to the salary range, we offer medical insurance, sick and vacation time, retirement savings plans, and access to discounts and perks. Conditions Of Employment All applicants who accept an offer of employment must comply with the following conditions of employment: Background Check and Live Scan Employment Misconduct Legal Right to work in the United States Vaccination Policies Smoking and Tobacco Policy Drug Free Environment Misconduct Disclosure Requirement Additional conditions may apply: California Child Abuse and Neglect Reporting Act E-Verify Pre-Placement Health Evaluation Closing Statement The University of California is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, protected veteran status, or other protected categories covered by the UC Anti-Discrimination Policy. We are committed to attracting and retaining a diverse workforce and providing reasonable accommodations for applicants with disabilities. Consideration for Work Authorization Sponsorship Must be able to provide proof of work authorization. #J-18808-Ljbffr
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- ...Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard... ...statewide. To learn more about UC Irvine, visit The UCI Center for Clinical Research (CCR) is full service clinical trials unit serving a...SuggestedWork experience placementWork at officeLocal area
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Description The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The ideal candidate is an experienced professional or leader who...Local area- A leading healthcare provider in California is seeking a Clinical Research Coordinator II to manage patient coordination for clinical trials. This role involves screening patients, ensuring data accuracy, and adhering to regulatory compliance. The ideal candidate should...
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Children’s Hospital of Orange County is looking for a Clinical Research Coordinator II to support multiple human subjects’ clinical research projects. The role includes assessing protocol feasibility, coordinating research data collection, and participating in regulatory...Hourly pay$89.45k - $143.9k
Description The Senior Clinical Research Coordinator plays a critical role in the overall operational management of clinical research/trial/study activities from design, set up, conduct, through closeout. The ideal candidate is an experienced professional or leader who...Local areaFlexible hours- · Manages clinical trials, including those conducted through Contract Research Organizations (CROs)· May participate in developing and recommending operational strategies for clinical trials in collaboration with cross-functional teams· May serve as a mentor and provide...Contract workLocal area
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Headlands Research in California is seeking a Clinical Research Coordinator to manage multiple clinical trials from initiation to close-out. This full-time role requires at least one year of experience in coordinating Phase 2-4 clinical trials and proficiency in phlebotomy...Full time- ...remote work: California, Arizona, Nevada, Oregon, Texas, Colorado, Minnesota, Florida, and Georgia. Cedars-Sinai is seeking a Clinical Research Finance Coordinator II (Pre-Award) to join our dynamic research team. In this role, you will be responsible for the financial...Contract workWork at officeLocal areaRemote work
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