Clinical Trial Manager
UCI Health
Your Role on the Team The Clinical Trial Manager will serve as the senior scientific leader responsible for designing, developing, and overseeing high‑quality clinical research programs within the Susan Samueli Integrative Health Institute (SSIHI). The role includes lead protocol conception and authorship, sponsor engagement, feasibility assessment, and ensuring rigorous scientific and operational outcomes. The manager will collaborate closely with investigators, regulatory agencies, data science partners, IT and compliance teams, and external sponsors to integrate advanced analytics, predictive modeling, and real‑world data into study designs. Required Qualifications In‑depth knowledge of research functions and scientific methodology. Advanced statistical analysis, database management, and systems programming skills. Advanced project management abilities, with experience leading and influencing cross‑functional teams. Strong communication skills, able to convey complex information clearly in both written and verbal formats. PhD (or equivalent doctoral degree) in clinical research, epidemiology, biostatistics, biomedical informatics, data science, health sciences, or a related field. Preferred Qualifications Knowledge or experience in integrative and/or functional medicine research. Benefits In addition to a competitive salary range, the position offers a comprehensive benefits package that may include medical insurance, paid sick and vacation time, retirement savings plans, and various employee discounts and perks. Conditions of Employment Background check and live scan. Compliance with a drug‑free environment policy. Vaccination policies and smoking/tobacco policies. Legal right to work in the United States. Employment misconduct disclosure requirements. California Child Abuse and Neglect Reporting Act. E-Verify participation. Pre‑placement health evaluation. Equal Opportunity & EEO Statement The University of California, Irvine 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 diversity, equity, and inclusion in all aspects of employment. Work Authorization Sponsorship Must be able to provide proof of work authorization. #J-18808-Ljbffr UCI Health
- ...well-being practices, providing individualized, patient-centered clinical care, and providing services to the community that focus on obtaining optimal health. Responsibilities The Clinical Trial Manager will serve as the senior scientific leader responsible for designing...SuggestedLocal area
- ..., educating the public on well-being practices, providing individualized clinical care, and offering community services focused on optimal health. Your Role on the Team The Clinical Trial Manager will serve as the senior scientific leader responsible for designing, developing...Suggested
- ...Technology & Telecom is seeking a candidate to provide financial support for Clinical Research Departments in Irvine, California. The role involves assisting with Clinical Study financial tasks, managing Purchase Orders, and ensuring accurate payment reconciliation. Ideal...Suggested
- City of Hope is seeking a Clinical Study Coordinator in California to support oncology clinical trials from First in Human to Phase III. You will coordinate recruitment, informed consent, data management, and regulatory compliance while collaborating with investigators...Suggested
$25 per hour
...Clinical Research Recruitment Coordinator Irvine Clinical Research is the largest independent... ...of people each year. Every research trial brings us closer to finding a treatment... ...of your work responsibilities Time management skills to coordinate and manage recruitment...SuggestedHourly payFull timeLocal areaRemote work$35 - $38 per hour
...New Clinical Research Coordinator Opportunity This Jobot Consulting Job is hosted by: Stephen Williams Are you a fit? Easy Apply... ...organizational skills, attention to detail, and the ability to manage multiple priorities in a fast-paced healthcare environment....Hourly payWork at officeLocal area$28 - $40 per hour
...Job Title: Clinical Research Coordinator - Dermatology Trials Job Description The Clinical Research Coordinator leads and manages dermatology industry-initiated clinical trials in a high-volume private practice and research setting. This role oversees 11-15 concurrent...Full timeContract workTemporary workPrivate practiceMonday to Friday- ...UC Irvine Health is seeking an Assistant Clinical Research Coordinator to support cancer research committees and maintain clinical trial information. The successful candidate will coordinate high-level meetings, assist Principal Investigators, and ensure compliance with...
$117k - $201.25k
...their merit.Job Function: Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function:... ...currently recruiting for a Clinical Research Manager. This role is located in Irvine, CA on a... ...execute and manage company sponsored clinical trials, ensuring monitoring compliance with...Full timeFor contractorsInterim roleLocal areaImmediate start2 days per week3 days per week$117k - $201.25k
...their merit.Job Function: Discovery & Pre-Clinical/Clinical DevelopmentJob Sub Function:... ...for a Clinical Science & External Research Manager to support the Electrophysiology (EP) business... ...including the investigator sponsored trial program ensuring high adherence to SOPs,...Full timeLocal areaImmediate start- The Clinical Research Coordinator (CRC) is responsible for the day‑to‑day coordination and... ...hands‑on experience coordinating clinical trials, including participant screening, eligibility... ..., and safety reporting. The CRC will manage 5-10 active studies simultaneously and work...
- Are you interested in working in clinical research? Do you have a background in nursing or... ...investigators in recruiting and management research studies directly affecting the... ...RESPONSIBILITIES: Develops and outlines trial protocols. Develops and maintains site...Work experience placementPrivate practiceWork at office
$24 - $32 per hour
Future Opening: Clinical Research Coordinator II Full Time • Garden Grove The National Institute of Clinical Research (NICR) is an independent, multi-site clinical trial site management organization (SMO). We deliver and facilitate the highest quality Phase 1 - 4 trial...Hourly payFull timeWork at officeLocal area- ...Clinical Trials Data Coordinator - Remote Join the transformative team at City of Hope , where we're changing lives and making a real difference in the fight against cancer, diabetes, and other life-threatening illnesses. City of Hope's growing national system...Full timeLocal areaRemote work
$70k - $75k
Clinical Research Coordinator | Temp to Hire | $$$$ Jobot Consulting Job is hosted by: Ba Tran Salary: $70,000 - $75,0... ...the healthcare industry. You will play a crucial role in managing and overseeing clinical trials, ensuring they are conducted in accordance with ethical...Temporary workLocal area$32 - $35 per hour
Job Title: Clinical Research Coordinator (CRC) Job Type: Full-Time Job Location(s): Orange... ...includes FDA-regulated drug and device trials, NIH-funded research, and investigator-... ...ensure protocol adherence. Participant Management Recruit, screen, and consent...Full timeRelocation- ...CA (Training will be in Glendale for 6-9 weeks) Overview The Clinical Research Coordinator works independently providing study coordination... ...patients for protocol eligibility, presenting non-medical trial concepts and details, and participating in the informed consent...Local area
- ...of Neurology is committed to advancing clinical care, education, and research to help patients... ...for comprehensive coordination and data management of a diverse portfolio of research... ...clinical study information in the clinical trial management system (OnCore) and adhere to...Full timeWork experience placementWork at officeLocal areaRemote work
$19 per hour
Job Summary We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory...Hourly payFull timeWork at officeMonday to FridayShift workWeekend work$75k - $105k
Regional Travel, Clinical Research Coordinator Huntington Beach, California, United States... ...in all aspects of conducting clinical trials Maintain effective relationships with study... ...and Care Access Research personnel and management Coordinate and attend pre‑study site...Full timeTemporary workWork at officeLocal areaVisa sponsorshipWork visaFlexible hours- ...health of our community’s pediatric population in our hospitals, clinics, and practices. And because of our breadth of care, your... ...responsibilities for human subjects’ (clinical) research. Study management includes but is not limited to assisting in assessing feasibility...Full timeWork at officeShift work
$37.56 per hour
...duties include, but are not limited to: Independently manage the regulatory lifecycle of clinical research studies, including study activation, IRB... ...requirements for Phase I-III drug and device clinical trials. Experience working in a healthcare or clinical research...Full timeTemporary workPart timeWork experience placementLocal areaMonday to FridayAfternoon shift$90k - $100k
...considered.*** Job description Job Title: Senior Clinical Research Coordinator (Liver Trials) Job Type: Full-Time | On-Site Job Location:... ...including screening, enrollment, and follow-up • Manage regulatory submissions (IRB, CPHS), source...Full timeRelocationRelocation package- ...Job Title: Manager, Clinical Research Affairs Role Level: People Manager Supervisor/Manager Title: Director, Clinical Affairs Job... ...of high-level site management activities across clinical trials. This individual plays a critical role in ensuring data quality...Full timeWork at office
$125k - $150k
...party auditing and certification services, including food safety, animal welfare, and GMP programs. Position Overview The Laboratory Manager is responsible for leading the day‑to‑day operations of the laboratory to ensure the accuracy, reliability, and timeliness of...Contract workWork at office$26.5 - $28.5 per hour
...on-site labs, and programs for preventive care, chronic care management, common illnesses and mental health concerns have been delighting... ...serves as the practice team’s main point of contact for daily clinical operational oversight. You will motivate, support, and under...Hourly payFull timeTemporary workWork at officeMonday to FridayShift work- ...What You'll Do: The Clinical Project Manager / Senior Project Manager is part of this group and will be working closely with the Clinical... ...project plans, timelines, and resource allocation for clinical trials and related activities ~ Facilitate cross functional...Full timeLocal areaShift work
$115k - $135k
...relevant experience to a new industry, join our team as we help shape a brighter way forward. What this job involvesSupporting and managing industry changing projectsAs a Project Manager at JLL, you will be directly responsible for working with a team to deliver complex...Full timeLocal area$90k - $120k
...Paid time off ~ Vision insurance ~401(k) matching ~ Dental insurance Position Summary We are seeking a Clinical Research Program Manager to help develop and support the clinical outcome research program in mental health and substance use at Pacific Neuropsychiatric...Work at office$50 per hour
...Job Description Job Description Clinical Research Coordinator-RN II needed at hospital in Newport Beach, CA... ...stakeholders, and sponsors. The position is responsible for managing complex clinical research trials including drug, device, and biologic studies across...Contract workLocal areaRemote work
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