Senior Director, Global Pre-Approval Patient Access

About the role

This role will lead operational priorities where safety, quality, compliance, and execution discipline are central to success. You will collaborate with field leadership, support functions, and cross-functional stakeholders to improve accountability, service delivery, and operational consistency. The position offers the opportunity to influence operational scale, customer outcomes, and organizational performance within a life sciences environment.

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

Responsibilities

• Develop and implement enterprise-wide strategy for early access programs
• Design and coordinate free-of-charge named-patient and cohort access initiatives globally
• Lead cross-functional collaboration among Clinical, Regulatory, and other departments
• Establish governance for evaluating and prioritizing new early access programs
• Oversee program operations and manage vendor relationships
• Create company-wide policies for ethical access decisions
• Collaborate with Development on early access planning aligned with lifecycle strategies

Qualifications

• Bachelor's degree in a healthcare field (advanced degree preferred)
• 12+ years of clinical trial operations and oncology early access experience
• Proven track record of designing and executing global early access programs
• Deep knowledge of global regulatory authorities' programs and timelines
• Strong organizational skills with a proactive, resourceful approach
• Experience leading large cross-functional teams with a collaborative mindset
• Ability to manage complex issues and deliver high-quality solutions

Pay

$232,000 – $290,000 annually

Benefits

• Robust equity awards
• Strong benefits package
• Extensive learning and development opportunities