University of California, Irvine

Temporary Clinical Research Coordinator


PayCompetitive
LocationIrvine/California
Employment typeFull-Time

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  • Job Description

      Req#: 100026
      Employer Industry: Higher Education and Clinical Research

      Why consider this job opportunity:
      - Salary range of $33.08/hour - $34.48/hour
      - Comprehensive benefits including medical insurance, paid vacation, sick leave, and retirement savings plans
      - Opportunity to work in a prestigious university environment with a focus on innovative research
      - Engage with diverse teams and contribute to impactful clinical trials
      - Temporary employment with potential for flexible hours and varied assignments

      What to Expect (Job Responsibilities):
      - Manage 5–7 clinical trials, coordinating study activities, subject visits, and ensuring protocol adherence for approximately 6–8 patients per trial
      - Support patient recruitment, screening, consenting, and data collection in collaboration with the Assistant Clinical Research Coordinator and Principal Investigator
      - Serve as the main liaison between employer Health staff, campus departments, and study sponsors to ensure smooth communication and operations
      - Prepare and submit regulatory documents to the IRB, SPA, and other entities, and assist with sponsor monitoring visits or audits
      - Maintain accurate study records, research charts, and compliance documentation in alignment with clinical trial requirements

      What is Required (Qualifications):
      - Bachelor's or Master's degree, preferably in biology or life sciences
      - 3-5 years of previous clinical trial experience
      - Previous experience with participant recruitment
      - Ability to read, write, and follow written and oral instructions in English
      - Compliance with conditions of employment including background check and vaccination policies

      How to Stand Out (Preferred Qualifications):
      - Experience with regulatory documentation and compliance in clinical research
      - Familiarity with data collection and management software
      - Strong organizational and multitasking skills
      - Excellent interpersonal and communication skills
      - Ability to work independently and as part of a team

      #HigherEducation #ClinicalResearch #TemporaryEmployment #CareerOpportunity #DiversityAndInclusion

      "We prioritize candidate privacy and champion equal-opportunity employment. Central to our mission is our partnership with companies that share this commitment. We aim to foster a fair, transparent, and secure hiring environment for all. If you encounter any employer not adhering to these principles, please bring it to our attention immediately. We are not the EOR (Employer of Record) for this position. Our role in this specific opportunity is to connect outstanding candidates with a top-tier employer."
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