Senior Manager, Post Trial Supply

Role Overview

• Responsible for facilitating continued access to sponsor medications for patients transitioning out of parent protocols through Patient Programs and PTS pathways
• Collaborate cross-functionally to ensure compliance with PTS processes
• Streamline operations and enhance patient access globally
• Support implementing new or revised Global Clinical Operations policies
• Provide guidance and support to cross-functional teams
• Collaborate with key stakeholders and external vendors
• Set up and maintain CyberGrants and manage budgets
• Ensure pharmacovigilance compliance by maintaining project documentation
• Manage program milestones and timelines
• Identify emerging risks and regulatory concerns

Requirements

• Bachelor or higher degree in a scientific or healthcare discipline
• At least 7 years’ relevant healthcare experience
• 5+ years of leadership experience
• 3+ years of leadership experience managing senior manager level above persons
• Proficiency in MS Office Suite, including Excel, PowerPoint, and Project
• Project management and/or project supporting experience across multi-region/country clinical trials in a global environment preferred.

Benefits

• Medical
• Dental
• Vision
• 401(k)
• FSA/HSA
• Life Insurance
• Paid Time Off
• Wellness
• Opportunity to own shares of BeOne Medicines Ltd. stock
• Discretionary equity awards
• Participation in Employee Stock Purchase Plan