Description
The role supports global EDC solutions by managing contractual and validation documentation, assisting with study and controlled-document creation, production, printing, and tracking, executing validation test scripts, maintaining validation metrics, and ensuring quality and compliance with Fortrea SOPs, Quality Management, and GCP/ICH guidelines. It requires a life sciences, health sciences, information technology, or related degree or allied-health certification, fluent English, and 2–4 years of CDM and EDC testing experience with Rave and Veeva expertise. The position is remote and may require flexible shift-based working hours.
