Global Clinical Process Management Senior Specialist

Role: Support process management and operational coordination within GCPM to facilitate effective execution of governance, document control, and process improvement activities in a biopharma setting. Responsibilities: assist process leads with document review workflows, document control, project plan updates, stakeholder communication, and organizational change activities; support senior management with data compilation from systems like Veeva Vault, and tracking of CAPA and intake data for process review and innovation. Requirements: Bachelor’s degree; 2+ years in pharmaceutical or biotech industry preferred; proficiency in Microsoft Office Suite; knowledge of ICH-GCP; strong organizational, communication, and problem-solving skills. HighValue: focused on clinical process support, GCP compliance, document workflows, and process improvement within a biopharma environment. No travel required. Work setup: unspecified.