Content Management Specialist (Pharmaceuticals) - Tieto Tech Consulting (m/f/d)
Hybrid
Core
Manage study requirements, configuration files, and content delivery for clinical studies in a pharmaceutical context.
Role type
Content Management Specialist (Clinical Studies)
Builds
Clinical study content and configuration files
Domain
Pharmaceuticals / Clinical Trials
Required skills
CMS platforms, content operations, pharma/clinical terminology, cross-browser testing, stakeholder coordination, deadline management
Preferred skills
Contentstack, BrowserStack, clinical study content experience
Responsibilities
Manage study requirements and configuration files, Create and update content in CMS platforms, Coordinate content preparation and deployment, Validate content across browsers, Work with pharma and clinical terminology, Manage multiple priorities and tight deadlines
Seniority
Individual Contributor
