Clinical Trial Coordinator

6 days ago


San Diego, California, United States Abbott Full time
Job Description

We are seeking a skilled Clinical Research Associate to join our team at Abbott. As a member of our team, you will be responsible for conducting monitoring visits and activities in accordance with FDA Code of Federal Regulations, GCP guidelines, departmental SOPs, Work Instructions, and the Clinical Monitoring Plan.

About the Position

In this role, you will serve as the primary site contact, establishing and maintaining regular communication with clinical sites. You will also assist with distribution, collection, and tracking of regulatory documents for site compliance and audit readiness.

Responsibilities
  • Conducting monitoring visits and activities in accordance with FDA Code of Federal Regulations, GCP guidelines, departmental SOPs, Work Instructions, and the Clinical Monitoring Plan.
  • Serving as primary site contact; establishing and maintaining regular communication with clinical sites.
  • Assisting with distribution, collection, and tracking of regulatory documents for site compliance and audit readiness.
Requirements

This position requires working knowledge of clinical trial practices and regulations, clinical trial databases, proficient computer skills including Microsoft Office Suite, minimum BA or BS and 2 years of related clinical trial monitoring experience, on-site monitoring experience of IVD clinical studies is preferred.

Estimated Salary

$83,400 - $152,400 per year, depending on location.



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