Associate Director, Global Regulatory Project Management and Strategic Planning - Oncology

Location: Remote – US-based candidates only, no visa sponsorship available

Compensation: $154,400 – $242,550 annually

About the role

This role will drive complex programs from planning through execution with a focus on structure, accountability, and measurable delivery. You will work across business leaders, delivery teams, and strategic partners to align priorities, manage dependencies, and keep initiatives on track. The position offers the opportunity to bring clarity to complex work and deliver outcomes that matter across the organization within a life sciences environment.

Responsibilities

• Collaborate with Global Regulatory Lead (GRL) to direct Global Regulatory Teams (GRT) and ensure project goals are met
• Lead cross-functional submission working groups to achieve successful Health Authority submissions
• Provide ongoing regulatory operational support for assigned programs, ensuring effective vendor management
• Proactively manage and facilitate project teams, maintaining focus on deliverables and problem-solving
• Report on regulatory milestones, critical issues, and risk management to stakeholders

Requirements

• Bachelor's degree required, preferably in Science; advanced degree preferred
• Minimum of 8 years experience in Regulatory Project Management; 4 years in Global Regulatory Affairs preferred
• Experience with late-stage filings highly preferred
• Advanced credentials in regulatory affairs and project management are a plus
• Significant knowledge of global drug development regulations and lifecycle management

Benefits

• Work alongside experienced professionals in an innovative environment
• Opportunity for continuous improvement and process implementation
• Training and mentorship opportunities for career advancement