Job Title: Freelance Senior Clinical Research Associate
Job Location: UK (Home-based)
Job Overview:
The Contract Sr. Clinical Research Associate monitors investigational sites to ensure subject safety and provide high-quality data review and reporting in compliance with the Caidya and/or client Standard Operating Procedures (SOPs), Good Clinical Practice (GCP)/ International Conference on Harmonization (ICH) guidelines, ISO14155, and other applicable local regulations. Builds, manages and supports strong site relationships while liaising between the Sponsor and assigned sites.
Job Duties and Responsibilities:
Supervisory Responsibilities: None
Job Requirements:
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