Regulatory Affairs Coordinator

17 hours ago

Orange, California, United States University Of California Irvine Full time
Overview

The University of California, Irvine is seeking a highly skilled Assistant Regulatory Affairs Coordinator to join our team. As a key member of our Center for Clinical Research, you will play a critical role in ensuring the successful management of regulatory aspects of clinical trials.

Responsibilities
  • Work closely with the Lead Regulatory Coordinator to ensure compliance with regulatory requirements and guidelines.
  • Manage and maintain accurate and up-to-date records of regulatory documents and submissions.
  • Coordinate with study sponsors, CROs, PIs, and other stakeholders to ensure seamless communication and collaboration.
  • Develop and implement processes to improve efficiency and effectiveness in regulatory affairs.
  • Provide training and support to team members on regulatory policies and procedures.
Requirements
  • Bachelor's degree in a related field or equivalent experience.
  • Basic understanding of clinical trials and research.
  • Excellent communication and problem-solving skills.
  • Ability to work in a fast-paced environment and prioritize multiple tasks.
  • Proficient in Microsoft Office and ability to generate reports and documents.
Preferred Qualifications
  • CCRP certification or equivalent experience.
  • Clinical research experience preferred.
What We Offer

The University of California, Irvine offers a competitive salary range of $26.6-$43.82 per hour, as well as a comprehensive benefits package, including medical insurance, sick and vacation time, retirement savings plans, and access to discounts and perks.

Conditions of Employment

The University of California, Irvine is an Equal Opportunity/Affirmative Action Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, age, or protected veteran status.

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