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Director, Portfolio Development Process & Standards Lead

CSL
September 01, 2026
Full-time
Remote friendly (King of Prussia, PA)
Worldwide
Clinical Research and Development
Role: Director, Portfolio Development Process & Standards Lead, overseeing global portfolio development frameworks ensuring quality and compliance. Responsibilities: manage SOP updates across Portfolio Development; develop technical training curricula; guide process and stakeholder management; lead process improvement initiatives; ensure procedural document compliance; represent Portfolio Development in cross-functional R&D forums; drive technology integration and process excellence. Requirements: Bachelor's in life sciences or related field; 12+ years in biotech/pharma with deep drug development and GCP knowledge; 5+ years managing clinical R&D projects; 3+ years leading process improvements and change management; experience leading multicultural, international teams. HighValue: 12+ years biotech/pharma experience, clinical trial execution, process improvement, cross-functional team leadership, GCP environment expertise. WorkSetup: hybrid roles in PA, MA, or UK; three days onsite.