Description
Parexel is hiring a Systems Validation Specialist to work remotely in Argentina or Mexico. The role supports the definition, adoption, and oversight of compliant quality and technology processes for clinical research and drug development, including computerized system validation, quality frameworks, project quality oversight, continuous improvement, audits, GxP guidance, risk mitigation, and quality issue management. Candidates need at least three years of clinical research or clinical trial experience with GCP and technology compliance, familiarity with system lifecycle and GCP regulations, and intermediate Microsoft Office and Adobe PDF skills.
