UCI Health
Who We Are
Founded in 1965, UC Irvine is a member of the prestigious Association of American Universities and is ranked among the nation’s top 10 public universities by U.S. News & World Report. The campus has produced five Nobel laureates and is known for its academic achievement, premier research, innovation and the anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs. It is Orange County’s second‑largest employer, contributing $7 billion annually to the local economy and $8 billion statewide. For more information, visit
www.uci.edu .
UCI Alpha Clinic Overview
Part of the California Institute for Regenerative Medicine (CIRM) Alpha Clinic network
Promotes and facilitates scientific collaborations and interactions
Provides centralized clinical research infrastructure support for cell and gene therapy clinical trials
Accelerates the implementation of cell and gene therapy clinical trials at UCI
Senior Clinical Research Coordinator Role Under the direction of the Assistant Director of Clinical Research Operations, the Senior Clinical Research Coordinator will support UCI Alpha Clinic (AC) clinical research efforts by providing comprehensive coordination and data management of sponsored clinical trials according to Good Clinical Practices (GCP), internal standard operating procedures (SOPs), and University policies and procedures. The incumbent will support and coordinate all aspects of UCI AC trials and studies for protocol‑specific requirements, research procedures, chart preparation, data collection, subject study management, and record keeping. The coordinator will attend clinic to assist the Principal Investigator (PI) with recruitment, screening, consenting, administering questionnaires, and other study tasks. The coordinator will ensure study protocols are followed, appropriate documentation is kept, and accurate data is collected. The coordinator will prepare and submit study documents to the Institutional Review Board (IRB), Sponsored Projects Administration (SPA), and other regulatory committees.
Qualifications and Experience
High‑level communication skills and ability to present information clearly and concisely
Problem‑solving capabilities to resolve unexpected concerns
Research skills, including evaluation of information and preparation of concise, well‑organized reports and summaries
Organizational skills, ability to prioritize a complex and dynamic workload, multitask, and meet deadlines
Judgment and discretion, ability to work collegially within a small office, and foster cooperative relationships
Ability to work independently, take initiative, follow through on assignments, and think critically to compile data from various sources
High integrity, honesty, confidentiality, and professional appearance with strong attention to detail
Working knowledge of Microsoft Office (Outlook, Word, Excel, PowerPoint)
Bachelor’s degree in a related area and/or equivalent experience/training; national clinical research coordinator certification preferred
3‑5 years of experience required; advanced degree (MA, MS, MPH) preferred
Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals preferred
Preferred Qualifications
Advanced degree (MA, MS, or MPH)
Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals
Experience in cell and gene therapy clinical trials (preferred)
Conditions of Employment
Background check and live scan required
Compliance with employment conduct policies, including misconduct disclosure and suspicion policies
Vaccination policy adherence and drug‑free environment
Flexibility for occasional evening and weekend work hours
Commitment to Diversity and Equal Opportunity The University of California, Irvine is an Equal Opportunity / Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or protected veteran status. UCI provides reasonable accommodations for applicants with disabilities upon request. For more information, please contact Human Resources at (949) 824‑0500 or eec@uci.edu. The University of California, Irvine is an Equal Opportunity / Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age or protected veteran status. For the University of California’s Anti‑Discrimination Policy, please visit https://policy.ucop.edu/doc/1001004/Anti‑Discrimination. We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable, and welcoming.
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www.uci.edu .
UCI Alpha Clinic Overview
Part of the California Institute for Regenerative Medicine (CIRM) Alpha Clinic network
Promotes and facilitates scientific collaborations and interactions
Provides centralized clinical research infrastructure support for cell and gene therapy clinical trials
Accelerates the implementation of cell and gene therapy clinical trials at UCI
Senior Clinical Research Coordinator Role Under the direction of the Assistant Director of Clinical Research Operations, the Senior Clinical Research Coordinator will support UCI Alpha Clinic (AC) clinical research efforts by providing comprehensive coordination and data management of sponsored clinical trials according to Good Clinical Practices (GCP), internal standard operating procedures (SOPs), and University policies and procedures. The incumbent will support and coordinate all aspects of UCI AC trials and studies for protocol‑specific requirements, research procedures, chart preparation, data collection, subject study management, and record keeping. The coordinator will attend clinic to assist the Principal Investigator (PI) with recruitment, screening, consenting, administering questionnaires, and other study tasks. The coordinator will ensure study protocols are followed, appropriate documentation is kept, and accurate data is collected. The coordinator will prepare and submit study documents to the Institutional Review Board (IRB), Sponsored Projects Administration (SPA), and other regulatory committees.
Qualifications and Experience
High‑level communication skills and ability to present information clearly and concisely
Problem‑solving capabilities to resolve unexpected concerns
Research skills, including evaluation of information and preparation of concise, well‑organized reports and summaries
Organizational skills, ability to prioritize a complex and dynamic workload, multitask, and meet deadlines
Judgment and discretion, ability to work collegially within a small office, and foster cooperative relationships
Ability to work independently, take initiative, follow through on assignments, and think critically to compile data from various sources
High integrity, honesty, confidentiality, and professional appearance with strong attention to detail
Working knowledge of Microsoft Office (Outlook, Word, Excel, PowerPoint)
Bachelor’s degree in a related area and/or equivalent experience/training; national clinical research coordinator certification preferred
3‑5 years of experience required; advanced degree (MA, MS, MPH) preferred
Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals preferred
Preferred Qualifications
Advanced degree (MA, MS, or MPH)
Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals
Experience in cell and gene therapy clinical trials (preferred)
Conditions of Employment
Background check and live scan required
Compliance with employment conduct policies, including misconduct disclosure and suspicion policies
Vaccination policy adherence and drug‑free environment
Flexibility for occasional evening and weekend work hours
Commitment to Diversity and Equal Opportunity The University of California, Irvine is an Equal Opportunity / Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or protected veteran status. UCI provides reasonable accommodations for applicants with disabilities upon request. For more information, please contact Human Resources at (949) 824‑0500 or eec@uci.edu. The University of California, Irvine is an Equal Opportunity / Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age or protected veteran status. For the University of California’s Anti‑Discrimination Policy, please visit https://policy.ucop.edu/doc/1001004/Anti‑Discrimination. We are committed to attracting and retaining a diverse workforce along with honoring unique experiences, perspectives, and identities. Together, our community strives to create and maintain working and learning environments that are inclusive, equitable, and welcoming.
#J-18808-Ljbffr