University of California, Irvine
Temporary Clinical Research Coordinator (CRC)
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Job Description
- Req#: 121533
Employer Industry: Higher Education and Clinical Research
Why consider this job opportunity:
- Pay rate of $33.08/hour
- Comprehensive benefits including medical insurance, paid vacation, holidays, and sick leave
- Opportunity for career advancement and growth within the organization
- Work in a prestigious university environment with a focus on innovative research
- Engage in meaningful work that contributes to the advancement of medical knowledge and patient care
What to Expect (Job Responsibilities):
- Coordinate and manage clinical trials from initiation through completion, ensuring compliance with study protocols
- Conduct interviews with study patients, screen participants, and collect data in accordance with established protocols
- Develop processes for review and oversight of clinical trials, ensuring accurate documentation and data collection
- Compile and transcribe research patient data into case report forms and electronic data capture systems
- Collaborate with the clinical research team to manage data and assist Principal Investigators with data management tasks
What is Required (Qualifications):
- Minimum of 3 years of related work experience as a clinical research coordinator or assistant coordinator
- Proven experience in human subjects research coordination, including informed consent procedures and IRB submissions
- Familiarity with medical terminology and experience working in a medical/clinical setting
- Bachelor’s degree in a related area or equivalent combination of education and experience
- Valid California driver’s license and availability for travel to off-site research locations
How to Stand Out (Preferred Qualifications):
- SOCRA or ACRP Certification preferred
- Experience with Phase I, II, III drug trials, and device trials coordination
#ClinicalResearch #HigherEducation #CareerOpportunity #Healthcare #ResearchJobs
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