Cohortias, a CRO operating in Latin America, seeks a Computerized System Validation Specialist to lead validation lifecycle activities for GxP-regulated and eClinical systems. You will own compliance across our software and IT ecosystem, developing governance, validation plans, and CSA protocols.
The role requires 5-7 years in Pharma/CRO, strong knowledge of 21 CFR Part 11, EU Annex 11, ICH guidelines, and excellent English for integral audits.