Sr Director, Product Development Lead - 591

Role overview Lead global development programs for late-stage radiopharmaceutical treatments in oncology. The role aligns clinical, regulatory, manufacturing, quality, supply, and commercial teams around development plans, key decisions, and delivery milestones, while communicating program status and risks to senior leaders.

Responsibilities - Lead the cross-functional global program team and maintain the development plan and target product profile. - Coordinate planning across clinical, non-clinical, regulatory, quality, manufacturing, supply chain, commercial, medical affairs, and program management groups. - Drive governance, milestone readiness, change management, and documentation of decisions, including assessment of scope, schedule, and budget impacts. - Identify and manage program risks, assign owners, develop mitigations, and report issues with recommended actions. - Plan and forecast program budgets with Finance and functional leads, track spend, and recommend timely adjustments. - Shape regulatory development pathways and coordinate preparation for health authority interactions, including briefing materials and aligned responses.

Requirements - Demonstrated ability to lead complex, cross-functional development programs in a matrixed environment. - Strategic judgment, effective communication, and experience managing program risks and decisions. - Ability to maintain integrated plans, track milestones, and present clear, decision-focused status updates to senior stakeholders.

Nice to have - Direct people-management experience.

Benefits and work setup - Hybrid and remote arrangements are available across locations. - The source describes annual performance bonuses, equity-based incentives, vacation, paid wellness days, and learning and development support.