Job Details

Parexel seeks a Clinical Research Associate to act as the primary site contact and site manager for all phases of a clinical study. You will monitor sites to ensure data integrity and patient safety, manage regulatory documents, and support audits.

The role requires strong communication, travel, and a solid understanding of GCP/ICH guidelines. Applicants should have 2+ years of direct site monitoring experience in biopharma/CRO and a Bachelor's degree in science or biology.