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 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. Your Role on the Team 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 standard operating procedures (SOPs), and University policies and procedures. The incumbent is responsible for supporting and coordinating all aspects of the cancer‑related trials (Phase I‑IV) for protocol specific requirements, research procedures, research chart preparation, data collection, and record keeping. The coordinator attends clinic to assist the Principal Investigator (PI) with recruitment, screening, consenting, administering questionnaires, answering research patient questions, scheduling appointments, and other related duties. The coordinator serves as the liaison to sponsors and governing agencies and facilitates transmission of verbal and written communication to national cooperative oncology groups, pharmaceutical companies, and other research entities as needed. The incumbent is responsible for maintaining communication with all elements of a multi‑level research network, including attending Disease‑Oriented Teams (DOTs) meetings and interacting with sponsoring agencies such as the National Cancer Institute, and compliance and regulatory groups such as the Institutional Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors. The incumbent is responsible, under the direction of the CRM, to provide training and guidance to other clinical research coordinators, demonstrating best practices and providing ongoing analysis of internal processes with recommendations for new policies and procedures to improve overall operational efficiency and customer service. The incumbent is responsible, under the direction of the CRM, for leading and managing pre‑study site selection visits (PSSVs) and liaising with all appropriate ancillary medical service units (e.g., Investigational Drug Service, Pathology, Radiology, etc.) for the conduct of the trial for the assigned disease area. In addition, this individual must accurately maintain clinical trial information in the clinical trial management system (OnCore) and adhere to institutional policies and external Cancer Center Support Grant guidelines for reporting to the National Cancer Institute (NCI). What It Takes to be Successful 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 Demonstrated high‑level communication skills to convey information in a clear and concise way, synthesizing information and presenting it to others Demonstrated problem‑solving capabilities to resolve concerns that arise unexpectedly Demonstrated ability to research, properly evaluate information, and prepare concise, well‑organized reports, summaries, and correspondence Demonstrated ability to organize and prioritize a complex and dynamic workload Ability to multitask and meet deadlines, despite interruptions Ability to independently exercise discretion and sound judgment Ability to work collegially and cooperatively in a small office and to establish and maintain cooperative working relationships Demonstrated skill in interacting with persons of various social, cultural, economic and educational backgrounds Ability to prioritize assignments and achieve high productivity/quality with short time frames, under rigid deadlines, and /or in environments with frequent workload changes and competing demands Skill in working independently, taking initiative and following through on assignments Ability to think critically, compile data from various sources, analyze data, and prepare reports Ability to work both independently and as part of a team Ability to take initiative and demonstrate strong commitment to duties Ability to perform ongoing needs analysis and recommend solutions to resolve concern Ability to work within a deadline‑driven structure Demonstrated experience in maintaining flexibility and adaptability while implementing institutional change High level of integrity and honesty in maintaining confidentiality Foster and promote a positive attitude and professional appearance Strong attention to detail Working knowledge of computer software including Microsoft Office (Outlook, Word, Excel, and PowerPoint) required Bachelor's degree in related area and / or equivalent experience / training Certification by the Society of Clinical Research Associates or the Association of Clinical Research Professionals 5 to 7 Years of related clinical research coordination work experience with Bachelor of Arts/Bachelor of Science, or equivalent experience Experience with cancer‑related research Knowledge of various types of human subject clinical trials (e.g., National Group, industrial, and Investigator‑authored) Preferred Current nationally‑recognized clinical research coordinator certification (e.g., Society of Clinical Research Associates (SOCRA), Association of Clinical Research Professionals (ACRP), etc.) Experience with clinical trial management systems, preferably OnCore Special Conditions May require study management coordination outside of normal business hours May require travel to satellite sites Total Rewards 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. Conditions of Employment The University of California, Irvine (UCI) seeks to provide a safe and healthy environment for the entire UCI community. As part of this commitment, 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: As a condition of employment, the final candidate who accepts a conditional offer of employment will be required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining that they committed any misconduct; received notice of any allegations or are currently the subject of any administrative or disciplinary proceedings involving misconduct; have left a position after receiving notice of allegations or while under investigation in an administrative or disciplinary proceeding involving misconduct; or have filed an appeal of a finding of misconduct with a previous employer. The following additional conditions may apply, some of which are dependent upon business unit or job specific requirements: California Child Abuse and Neglect Reporting Act E‑Verify Pre‑Placement Health Evaluation Details of each policy may be reviewed by visiting the following page - 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 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. UCI provides reasonable accommodations for applicants with disabilities upon request. For more information, please contact Human Resources at View phone number on click.appcast.io or View email address on click.appcast.io. Consideration for Work Authorization Sponsorship Must be able to provide proof of work authorization. #J-18808-Ljbffr