University of California, Irvine
Temporary Clinical Regulatory Affairs Coordinator
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Job Description
- Req#: 103174
Employer Industry: Higher Education and Research
Why consider this job opportunity:
- Salary up to $34.48/hour
- Comprehensive benefits including medical insurance, sick and vacation time, and retirement savings plans
- Opportunity for career advancement within a prestigious university setting
- Engaging and collaborative work environment in the clinical research field
- Flexible scheduling options, including part-time, weekend, and evening hours as needed
What to Expect (Job Responsibilities):
- Manage the regulatory aspects of clinical studies conducted through the employer's Center for Clinical Research
- Oversee IRB review submissions and maintain approval documentation
- Maintain accurate documents, files, and OnCore records
- Collaborate with research teams to ensure compliance with regulatory standards
- Assist in preparing reports and documentation for regulatory audits
What is Required (Qualifications):
- 2-3 years of experience in regulatory affairs, IRB, and/or clinical research
- Ability to read, write, and follow written and oral instructions in English
- Strong attention to detail and organizational skills
- Capability to work independently and as part of a team
- Proficiency in managing multiple tasks and meeting deadlines
How to Stand Out (Preferred Qualifications):
- Familiarity with clinical trial processes and regulatory requirements
- Experience with OnCore or similar clinical research management systems
- Strong problem-solving skills and ability to adapt to changing regulations
- Previous experience in a university or research environment
- Excellent communication skills, both written and verbal
#HigherEducation #ClinicalResearch #RegulatoryAffairs #CareerOpportunity #CompetitivePay
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