Director, Process Optimization Lead

Role: Lead the Program and Study Management (P&SM) function within biopharma clinical operations, focusing on operational excellence, process improvement, and strategic planning to support clinical studies. Responsibilities include managing initiatives, optimizing processes, shaping P&SM strategy, and fostering cross-functional collaboration across GCO teams. The role involves driving innovation, enhancing team capabilities, and ensuring compliance with regulatory standards like ICH/GCP. Qualifications: Bachelor's degree or higher in life sciences, with 10+ years in clinical or drug development, including at least 8 years in project management, clinical monitoring, or startup roles in biotech/pharmaceutical/CRO settings. Proficiency in MS Office, strategic thinking, and leadership skills are essential. Preferred: experience in oncology or other therapeutic areas, global clinical operations, and leadership in process optimization. HighValue: Clinical development oversight, strategy alignment, process improvement, and leadership in a GxP environment. Stakeholder engagement is key, with travel as required. Work setup is not specified but involves global coordination.