Director of Clinical Research Administration & Finance
University of California, Irvine
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's 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, visitThe UCI Center for Clinical Research (CCR) is full service clinical trials unit serving a diverse array of clinical trials across 20 clinical departments, alongside the Stern Center for Clinical Trials and Cancer Research (cancer clinical trials) and the Alpha Clinic (cell and gene therapies). CCR is a large unit (approximately 70 staff), including clinical research coordinators, regulatory affairs, finance, and administrative positions. This unit is responsible for end-to-end coordination of interventional clinical trials and provides service support for non-interventional/minimal risk clinical trials across UCI's medical centers, clinics, and satellite sites in the Orange County region.
Your Role on the Team* With minimal supervision, the Director of Clinical Research Administration & Finance is directly responsible for all administrative operations encompassed within the UCI Center for Clinical Research. In partnership with the Medical Director and School of Medicine Dean's Office leadership, this position is responsible for developing short and long-range planning of administrative and financial goals and objectives regarding this clinical trials unit, including strategic support initiatives and other special projects.
* The Director of Clinical Research Administration & Finance serves in an advisory capacity to the Medical Director on all matters related to the UCI Center for Clinical Research's three main divisions: 1) clinical operations, 2) finance, and 3) business development and technology.
* The Director of Clinical Trials Administration & Finance serves as the main point of contact to other departments, the School of Medicine Dean's Office, Medical Center Offices as well as other campus offices and organizations and as administrative liaison for affiliated hospitals and external agencies.
Required:
- Broad knowledge of clinical research concepts, federal, state, and local laws and regulations, and industry requirements regarding the proper conduct of clinical trials. Broad theoretical and operational knowledge of clinical and patient safety standards and regulations relating to clinical research.
- Broad knowledge of all phases of clinical research, from study startup through closeout and primary publication and presentation. Knowledgeable about clinical studies involving complex trial design issues.
- Demonstrated management skills supervising, maintaining, and developing clinical staff within the study team, and acting as a mentor for professional staff and conducting reviews and performance evaluations. Effectively manages multiple important priorities.
- Demonstrated ability to work collaboratively with other cross-functional teams and people with a wide range of educational backgrounds. Demonstrated ability to interface with commercial, regulatory, federal, and other members of an extended study team. Ability to influence / persuade.
- Demonstrates excellent problem-solving and analytical skills. Creatively addresses complex or new problems. Proven skills to quickly evaluate complex issues and identify multiple options for resolution.
- Strong communicator; includes verbal and written, active listening, critical thinking, persuasiveness, advising and counseling skills. Skill in analyzing and presenting data and strategy to relevant team, governance, external consultant, and regulatory / oversight meetings.
- Demonstrated ability to organize research work functions in an efficient and effective manner. Great organizational skills applied to personal work and improving organization of assigned staff and trial.
- Innovative decision-making and judgment on a frequent basis entailing theplanning, development and implementation of new policies, procedures and situation solutions regarding cancer clinical research
- Experience working in a multidisciplinary matrixed work environment.
- Advanced degree in related area and / or equivalent experience / training
- Research certification (ACRP, SoCRA, or equivalent)
- 10+ years of relevant work experience with a Bachelor degree in related field, 5-7 years of relevant work experience with a Masters degree, or equivalent experience
Preferred:
- Broad academic knowledge and applied background in clinical research philosophy. Applies knowledge of theoretical concepts and business best practices in a trial setting. Proven ability to translate clinical research philosophy into direct and indirect clinical input to design, planning, initiation, execution, and reporting of clinical trials.
- Experience with the campus' clinical and research information and documentation application programs.
- Technical proficiency in project management software
Special Conditions:
- Some after business hours and occasional weekends
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.
- ...Organization providing our clients with healthcare administrative support. We provide services to Independent... ...team member for resolution as needed. Research health plan reimbursement policies and procedures, clinical guidelines, coding, and CCI edits to ensure claims...SuggestedWork at officeRemote workFlexible hours
- ...Clinical Research Supervisor 1 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...SuggestedWork experience placementLocal area
- ...achievement, premier research, innovation and anteater... ...The UCI Center for Clinical Research (CCR) is... ...direction of the Assistant Director of Clinical Research... .... Serving as an administrative and operational leader... ...May be responsible for finances, clinical operations,...SuggestedWork at officeLocal areaRemote work
- ...Primary Duties and Responsibilities The Supervisor of Clinical Research (SCR) assists in overseeing clinical research operational activities... ...and renewal of clinical research policies. Works with Director of clinical research on issues requiring problem-solving....SuggestedLocal area
$117k - $201.25k
...Clinical Research Manager Hybrid - Irvine, California, United States of America Salary: $117,000 – $201,250 (annual base) Our MedTech Electrophysiology clinical team is recruiting for a Clinical Research Manager located in Irvine, CA on a hybrid schedule of 2–3 days per...SuggestedFor contractorsInterim roleLocal area2 days per week3 days per week$117k - $201.25k
...dignity of our employees and recognize their merit. Job Function: Discovery & Pre-Clinical/Clinical Development Job Sub Function: Clinical Development & Research - Non-MD Job Category: People Leader All Job Posting Locations: Irvine, California...For contractorsInterim roleWork at officeLocal areaImmediate startRemote workFlexible hours2 days per week3 days per week$29 - $34 per hour
...About Us: Each of CenExel’s research sites specialize in Phase I to Phase IV clinical trials. Our Centers of Excellence comprise some of the most well respected... ...to maintain quality and compliance. Performs administrative and regulatory duties related to the study as appropriate...Full timeWork at officeMonday to FridayShift workNight shift- ...for its academic achievement, premier research, innovation and anteater mascot. Led by... ...Role on the Team Under supervision of the Clinical Research Manager of the Clinical Trials... ...Review Board (IRB), Food and Drug Administration (FDA), and sponsor monitors. In addition...Work experience placementWork at officeLocal area
- ...oversight for processing of claims/coding for clinical and infusion services team leadership.... .... Department & Schedule Department: Finance Schedule: M - F, 8:30 - 5:00 Location:... ...Bachelor’s degree in Healthcare Administration, Finance, or equivalent experience. Graduate...Local areaRemote work
- CenExel Clinical Research in Anaheim, CA is seeking a Clinical Research Coordinator to support coordination of clinical trials in adherence to ICH, GCP, protocol and company guidelines. The role includes data collection, safety assessments, regulatory duties, and close...
- ...WHAT YOU WILL DO The Clinical Administrative Coordinator provides a safe and professional environment when patients first enter our centers, where they are greeted and assisted in a positive and welcoming way. The Clinical Administrative Coordinator (CAC) is responsible...Full timePart timeWork at office
- Certified Group is a leading provider of laboratory testing, regulatory consulting, and certification & audit services across highly regulated industries. We are currently looking for a Chemist to join our growing team. ESSENTIAL RESPONSIBILITIES Perform analysis using...Temporary workWork experience placementFlexible hours
$24 - $32 per hour
...Future Opening: Clinical Research Coordinator II Full Time • Garden Grove The National Institute of Clinical Research (NICR) is an independent... ...study participants to ensure adherence to study protocols. Administrative Duties (may include, but not limited to) Collect, process,...Hourly payFull timeWork at officeLocal area$35 - $40 per hour
...Summary This role is responsible for coordinating and managing clinical research protocols under the authority of the Principal Investigator (PI) while ensuring compliance with all institutional and regulatory guidelines. It supports Ark management and patient recruitment...Hourly payFull time$32.12 - $52.92 per hour
...Your Role on the Team Under the direction of the Principal Investigator and Program Manager, the Clinical Research Coordinator supports the efforts of several research projects, including regional projects and national clinical trials with the opportunity to interface...Hourly payLocal area$50 per hour
...campuses are seeking a part‑time licensed clinical psychologist whose primary... ...The supervisor reports to the College Director of the Office of Placement and Training... ...with assistance regarding the selection, administration, and scoring of assessment tools. Support...Part timeWork at officeFlexible hours$21 - $22 per hour
Patient Coordinator (Medical Receptionist - Full Time): Anaheim, CA Schweiger Dermatology Group is one of the leading dermatology practices in the country with over 400 healthcare providers and over 170 offices in New York, New Jersey, Pennsylvania, Connecticut, Florida...Full timeWork at officeLocal areaMonday to FridayFlexible hoursWeekend workWeekday work$35.77 per hour
...Responsibilities This recruitment is for a Temporary Full-Time Clinical Research Coordinator positions through UCI's internal temporary... ...required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining...Full timeTemporary workPart timeMonday to FridayAfternoon shift$32.12 - $52.92 per hour
...direction of the Principal Investigator and Program Manager, the Clinical Research Coordinator supports the efforts of several research... ...required to disclose if they have been subject to any final administrative or judicial decisions within the last seven years determining...Hourly payLocal area- ...Company Description M3 Wake Research, an M3USA Company, is an integrated network of premier investigational sites meeting the clinical research needs of global biopharmaceutical, biotechnology, medical device, pharmaceutical and clinical research organizations (CROs)....Flexible hours
- ...network of high-quality dermatology clinics that focus on collaborative and... ...is responsible for perfoming all administrative aspects of clinical trial research studies based upon needs and... ...and appropriate agencies. Notifies Director, sponsor and IRB of any serious adverse...Work at office
- ...Executive Medical Director About the Company Small, agile development team advancing... ...-phase immunology and inflammation clinical programs. Industry... ...Hiring Manager Title CSO Functions ~ Medical Care/Hospital Administration...Remote workFlexible hours
$25 per hour
...About Irvine Clinical Research Irvine Clinical Research is the largest independent memory research center on the West Coast. Alzheimer’s Disease is a serious cognitive illness that affects millions of people each year. Every research trial brings us closer to finding a...Hourly payFull timeLocal areaRemote work- CenExel is seeking a Clinical Research Coordinator in Anaheim, California. The role involves coordinating clinical trials while adhering strictly to ICH and GCP guidelines. Responsibilities include assisting with patient involvement, organizing trial information, and documenting...
- ...Subspecialty Faculty Leadership Opportunity at CHOC: Division Chief & Clinical Director, Thompson Autism and Neurodevelopmental CenterPosition:... ...for an experienced physician to guide the clinical, research, and educational mission of the Division of Neurodevelopmental...
- MemorialCare Health System is seeking a Clinical Research Coordinator I in Fountain Valley, California. This role involves recruiting, enrolling, and conducting follow-up for participants in clinical trials to ensure compliance with protocols and regulations. The successful...
$37.27 - $54.01 per hour
MemorialCare is seeking a Clinical Research Coordinator I to manage participant recruitment and ensure compliance with clinical trial protocols in Fountain Valley, CA. The role involves documenting study findings, coordinating participant care, and adhering to regulations...Full time- ...billing regulations and industry standards. High school diploma or equivalent required, Associates degree in Healthcare Administration, Medical Billing, or a related field preferred. In-depth knowledge of ambulance coding (HCPCS, ICD-10), billing procedures...Weekly payLocal area
- ...based medical aesthetics company with $350M+ in annual revenue, 400+ R&D engineers , and 100,000+ devices installed across 10,000+ clinics worldwide. We sit at the heart of innovation—bringing next-generation care to every community we serve. Our Mission Beauty with No...For contractorsWork at officeWorldwide
$115k - $130k
...workflows supporting chemical testing for personal care and cosmetic products. The Laboratory Manager partners closely with the Lab Director to support operational strategy while ensuring laboratory activities meet quality, regulatory, and client expectations. The...Work at office
Do you want to receive more vacancies?
Subscribe and receive similar vacancies to Director of Clinical Research Administration & Finance. Be the first to apply!
- healthcare consulting manager Orange, CA
- healthcare supervisor Orange, CA
- medicare medical director Orange, CA
- health economics manager Orange, CA
- director of health information management Orange, CA
- occupational health manager Orange, CA
- medical director oncology Orange, CA
- clinical nutrition manager Orange, CA
- medical coding manager Orange, CA
- director environmental health & safety Orange, CA

