Temporary Clinical Research Coordinator (CRC)
$37.56 per hourUC Irvine
Temporary Full-Time Clinical Research Coordinator PositionsFounded 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.This recruitment is for Temporary Full-Time Clinical Research Coordinator positions through UCI's internal temporary staffing service. Clinical research offices and clinics are located at the UCI Medical Center in Orange and the UCI campus in Irvine, as well as various clinics at community sites throughout Orange County.Job duties include, but are not limited to:Coordinate and manage Phase I–IV clinical trials from initiation through closeout, ensuring compliance with study protocols and timelines.Screen, interview, and enroll study participants; collect and document clinical data in accordance with established protocols.Oversee data management activities, including accurate entry into case report forms (CRFs) and electronic data capture (EDC) systems.Ensure adherence to Good Clinical Practice (GCP), internal SOPs, and university policies through ongoing monitoring and documentation oversight.What It Takes to be Successful:Required:Knowledge of clinical research processes, including trial coordination and human subject research regulations.3-5 years previous experience as a clinical research coordinator (CRC).Strong data management skills with attention to accuracy and detail in documentation and reporting.Ability to interpret and follow complex study protocols and regulatory requirements (e.g., GCP).Effective communication and organizational skills to coordinate with research teams and study participants.Ability to read, write, and follow written and oral instructions in English.Preferred:Bachelor's degree in related field or equivalent combination of education and experience.Experience supporting Phase I–IV clinical trials in an academic or healthcare setting.Familiarity with electronic data capture (EDC) systems and clinical research databases.Experience working with Principal Investigators and cross-functional research teams.Ability to develop and improve processes for study oversight and compliance.Total Compensation: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. Pay Rate: $37.56/hour.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 - Employment:This is a temporary employment recruitment reporting to the UCI Temporary Employment Services (TES) Department. Interviewing and hiring is based on internal hiring needs and how well the candidate's experience matches the assignment requirements.?Certain?temporary assignments may require clearance of a health physical or require a valid California Driver's License for driving university vehicles. The majority of our temporary positions are Monday – Friday, 8:00 a.m. – 5:00 p.m. We also have occasional part-time, weekend, and evening hours available, depending on the assignment. Comprehensive benefits options are also available for temporary employees, including paid vacation, holidays, and sick leave. Please note that we recruit for this position on an on-going basis to build a talent pool of potential candidates. When a position becomes available, we will review applicants at that time.?Due to the volume of applications that we receive, only those candidates selected for interviews will be contacted.?Thank you for your interest in employment with UCI Temporary Employment Services.Parking Information:All visitors, staff, and students are required to purchase parking permits to park on UCI property. If you plan to commute to work via your personal vehicle, I encourage you to review the parking requirements of your work location and parking rates on the UC Irvine Parking and Transportation websiteClosing 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
$90k - $100k
...Senior Clinical Research Coordinator (Liver Trials)Job Type: Full-Time | On-SiteJob Location: Orange, CAJob Salary: $90,000-$100,000 per year (based... ...POSITION. We're seeking a Senior Clinical Research Coordinator (CRC) with hands-on experience in liver-focused clinical trials....SuggestedFull timeRelocation$32 - $35 per hour
...Clinical Research Coordinator (CRC)Job Type: Full-Time Job Location(s): Orange, CA *This role is ONSITE* Job Salary: $32-$35/hour ($66,560.00 - $72,800.00 per year) Job Schedule: M-F 40-hours/week This is an on-site position in Orange, CA, and applicants must reside within...SuggestedFull timeRelocation- ...academic achievement, premier research, innovation and anteater... ...visit The UCI Center for Clinical Research (CCR) is driven to improve... ...(CCR). Serving as primary coordinator on trials of varying complexity... ...research coordinator (CRC) or an assistant CRC Demonstrated...SuggestedWork experience placementWork at officeLocal area
$24 - $35 per hour
...an accommodation or an alternative application process. Clinical Research Coordinator - Tustin, CA Full Time Tustin, CA, US 4 days ago Requisition... ...Position Overview The Clinical Research Coordinator (CRC) supports the conduct of clinical trial activities,...SuggestedHourly payFull time$24 - $32 per hour
...Future Opening: Clinical Research Coordinator II Full Time • Garden Grove The National Institute of Clinical Research (NICR) is an independent... ...to join our team as Senior Clinical Research Coordinator (CRC II). The CRC II is responsible for the management and coordination...SuggestedHourly payFull timeWork at officeLocal area- ...Clinical Research Coordinator IIWork Location: Orange, CaliforniaWork Shift: Evening – 08hrs (United States of America)At CHOC, we strive to be the... ...minimal supervision, the Clinical Research Coordinator II (CRC-II) is responsible for providing coordinator support to multiple...Work at officeShift workAfternoon shift
- Folio Clinical Research in Tustin, CA is seeking a Clinical Research Coordinator to support trial conduct, assist with lab processing, data entry, subject screening, recruitment... ...the PI/SI team. Ideal candidates have 1 year CRC experience (or 2 years as a Clinical Research...
- City of Hope is seeking a full-time, on-site Clinical Study Coordinator to support oncology trials at its Orange County location. You will manage patient recruitment, consent, data handling, and regulatory compliance in a fast-paced environment. Ideal candidates hold a...Full time
- UC Irvine’s Center for Clinical Research (CCR) seeks a Clinical Research Coordinator to lead day-to-day execution of assigned trials from initiation through close-out. The role involves coordinating data collection, CRFs, and communication with sponsors, IRB, FDA, and investigators...
$28 - $35 per hour
Clinical Research Coordinator - Newport Beach, CA Location: Newport Beach, CA (on-site); Additional site coverage needed for Mission Viejo, California... ...Job Description The Clinical Research Coordinator (CRC) is a specialized research professional working with and under...Full timeFlexible hours- MemorialCare Health System is seeking a Clinical Research Coordinator I in Fountain Valley to recruit, enroll and follow up on study participants across therapeutic areas. The CRC I will coordinate trial participation, track consent, and ensure protocol compliance with...
- The National Institute of Clinical Research (NICR) is an independent, multi-site Site Management Organization (SMO) conducting Phase I... ...clinical research. Position Summary The Clinical Research Coordinator (CRC) will play a key role in managing studies from initiation...Full timeLocal area
- ...Folio Clinical Research in Tustin, CA is seeking a Clinical Research Coordinator to support the conduct of clinical trial activities, ensuring regulatory compliance and aiding study operations across multiple trials. The role requires strong attention to detail, ability...
- ...Nobel laureates and is known for its academic achievement, premier research, innovation and anteater mascot. Led by Chancellor Howard... ...have reliable transportation to work in the different All of Us clinic locations around Orange County. Incumbent will be working on a...Work at officeLocal areaFlexible hours
$75k - $80k
...Clinical Research CoordinatorThe mission of The Los Angeles Cancer Network is to provide unparalleled care to each patient that comes through... ...the patients we serve.Job Description:The Clinical Research Coordinator works independently providing study coordination including...Local area- ...Job TitleSr. Clinical Research Regulatory CoordinatorJob DescriptionPrimary Duties And ResponsibilitiesThe Sr. Clinical Research Regulatory Coordinator supports clinical research teams (physicians, nurses, etc.) and with minimal direction and considerable use of independent...Full timeLocal area
- ...UC Irvine seeks a Clinical Research Coordinator to oversee human studies examining maternal stress and its effects on mother and child health. Responsibilities include participant screening, consent, visits, data management, regulatory compliance, and lab management of...
- ...UC Irvine is seeking an Assistant Research Data Coordinator to support CFCCC’s cancer trials. You will manage data collection, ensure quality control, and prepare CRFs for sponsor submissions using sponsor-specific EDC systems. You will collaborate with Principal Investigators...
- ...CHOC seeks a Clinical Research Coordinator II to support pediatric clinical research projects with minimal supervision. You will manage feasibility, regulatory submissions, participant identification, data collection, and record-keeping, ensuring compliance with policies...
- ...Are you interested in working in clinical research? Do you have a background in nursing or life sciences and are interested in bringing innovation... ...to help others? If so, a position as a clinical research coordinator might be the fit for you. Clinical Research Coordinators...Work experience placementPrivate practiceWork at office
- ...deployment, oversight, and maintenance of ECN Clinical processes in the conduct of clinical... ...and overall performance of a clinical research site. This role ensures that clinical trials... .... The Site Manager oversees site staff, coordinates resources, monitors key performance...Work at officeLocal areaMonday to Friday
$33.05 - $51.3 per hour
Description Under the supervision of the Medical Office Administrator, the Clinical Research Coordinator oversees the day to day functions of multiple clinical research studies. This role is responsible for interfacing with the Principal Investigator, Patient, Sponsor,...Daily paidMinimum wageWork at officeShift work- The Los Angeles Cancer Network is seeking a Clinical Research Coordinator to independently coordinate cancer trials, screen potential patients for protocol eligibility, and present non-medical trial concepts to participants during the consent process. You will manage source...
- A healthcare staffing company is seeking a Clinical Research Coordinator in Newport Beach, CA. Key responsibilities include assisting trial investigators, maintaining documentation, and ensuring compliance with research protocols. Ideal candidates will have 1-2 years of...Full time
- Providence Medical Foundation seeks a Clinical Research Coordinator to oversee the day-to-day functions of multiple clinical studies under the Medical Office Administrator. You will interface with the Principal Investigator, patients, sponsors, and the IRB to ensure timely...Work at office
- MemorialCare Health System in Fountain Valley, CA is seeking a Clinical Research Coordinator I to recruit, enroll and follow-up on participants in clinical trials across therapeutic areas. You will work under supervision to ensure protocol adherence, regulatory compliance...
- A medical practice specializing in eyecare is seeking a clinical research coordinator. Ideal candidates will have a bachelor’s degree in nursing or life sciences and 3+ years of relevant experience. Responsibilities include developing trial protocols, managing studies,...
$52 - $75 per hour
...based on patient schedule. The role requires an active California RN license and BLS certification with at least two years of clinical research experience. Oncology or CAR-T exposure is highly preferred. Compensation ranges from $52 to $75 per hour, commensurate with experience...Hourly payFull timeMonday to Friday$120k - $175k
...ease and professionalism. In addition, the candidate must have an active IL State Bar membership and demonstrate excellent legal research and writing skills. Why join us? Health Insurance Dental Insurance Vision Insurance 401K Job Details Responsibilities...Work at officeLocal area- About Profound Research Profound Research partners with community physicians to offer clinical trials as a therapeutic option for their patients. We handle all infrastructure... .... As an Assistant Clinical Research Coordinator at Profound Research, you’ll work alongside...Full timeContract workFor contractorsWork at office
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