Sr. Clinical Research Coordinator - Hybrid

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 anteater mascot. Led by Chancellor Howard Gillman, UC Irvine has more than 36,000 students and offers 224 degree programs.

It is located in one of the world’s safest and most economically vibrant communities and is Orange County's second largest employer, contributing $7 billion annually to the local economy and $8 billion statewide.

To learn more about UC Irvine, visit (Use the "Apply for this Job" box below)..

The NCI-designated Chao Family Comprehensive Cancer Center (CFCCC) is a campus-wide multidisciplinary matrix organization whose goal is to promote and enhance cancer-relevant research and patient care at UC Irvine. The CFCCC provides research resources to its ~175 members engaged in research and offers multidisciplinary cancer care to its patients.

Under the supervision of the Clinical Research Manager (CRM) within the Clinical Trials Unit, the Senior Clinical Research Coordinator (SCRC) supports the clinical research efforts of the Cancer Center by providing comprehensive coordination and data management for complicated Phase I-IV cancer protocols according to Good Clinical Practices (GCP), internal SOPs, and University policies and procedures.

The incumbent supports all aspects of phase I-IV trials including protocol specific requirements, research procedures, chart preparation, data collection, record keeping, clinic assistance, recruitment, screening, consenting, questionnaire administration, scheduling, sponsor liaison, regulatory compliance, training, pre‑study site selection visits, and accurate data entry in OnCore.

Required:

• Ability to interact with the public, faculty, and staff
• Ability to establish and maintain files and records
• Access to transportation to off‑site research locations
• Willingness to work as a supportive, cooperative member of an interdisciplinary team
• High‑level communication skills to convey information clearly and concisely
• Problem solving capabilities to resolve unforeseen concerns
• Research evaluation skills, concise report preparation
• Organizational skills to prioritize a complex dynamic workload
• Multitasking and deadline met skills
• Discretion and sound judgment
• Collaborative teamwork in a small office
• Skill to interact with diverse backgrounds
• Prioritization for high productivity under rigid deadlines
• Independent initiative and follow‑through
• Critical thinking and data analysis
• Independent and team work ability
• Initiative and commitment to duties
• Ongoing needs analysis and solution recommendation
• Deadline‑driven structure work
• Flexibility and adaptability with institutional change
• Integrity and confidentiality
• Positive attitude and professional appearance
• Strong attention to detail
• Computer skills including Microsoft Office (Outlook, Word, Excel, PowerPoint)
• 5 to 7 years of related clinical research coordination experience with a Bachelor of Arts/Science or equivalent
• Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals

Preferred:

• Experience with cancer‑related research
• Current nationally recognized clinical research coordinator certification (e.g., SOCRA, ACRP)
• Knowledge of various types of human subject clinical trials (National Group, industrial, investigator‑authored)
• Experience with clinical trial management systems, preferably On Core

• May require travel to satellite sites
• May require study management coordination outside normal business hours

In addition to the salary range listed below, we offer a wealth of benefits to make working at UCI even more rewarding. These benefits may include medical insurance, sick and vacation time, retirement savings plans, and access to a number of discounts and perks. Please utilize the links listed here to learn more about our compensation practices and benefits.

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