Senior Global Product Development Lead

🕒 June 24

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Telix Pharmaceuticals Limited

WebsiteLinkedInAll Job Openings

501 - 1000 employees

Founded 2015

🏥 Healthcare

💼 Consulting

🧬 Biotechnology

Healthcare • Consulting • Biotechnology

Telix Pharmaceuticals Limited is a commercial-stage biopharmaceutical company dedicated to transforming the way cancer and rare diseases are diagnosed and treated. Focusing on the development and commercialization of theranostic radiopharmaceuticals, Telix utilizes targeted radiation to enhance treatment decision-making and deliver personalized therapy. With an extensive pipeline addressing areas such as prostate and kidney cancer, neuro-oncology, and musculoskeletal cancers, Telix has garnered global regulatory approvals for its lead imaging agent, Illuccix®, and is actively conducting numerous clinical trials worldwide.

📋 Description

• Lead the Global Program Leadership Team (GPLT) and hold accountability for cross-functional commitments across CMC, Clinical, and Regulatory • Showcase courage in strategic thinking, guiding matrixed teams through complex decision-making and risk management processes • Foster a collaborative spirit, working seamlessly with teams spanning clinical, non-clinical, regulatory affairs, quality, manufacturing and supply chain, commercial, medical affairs and program management • Drive integrated cross-functional planning and confirm readiness for key milestones and inflection points • Identify, assign ownership of, and actively manage program risks/issues • Lead program-level budget planning and forecasting in partnership with Finance and functional leads • Partner with Clinical and Regulatory Affairs to craft the ideal development pathway for approval • Lead cross-functional preparation for key health authority interactions (e.g., FDA Type B) • Maintain clear, decision-focused reporting (dashboards, milestone tracking, red/amber/green risks) • Create and execute comprehensive product development plans and data packages • Partner with Technical Operations, Quality, and external vendors to ensure manufacturing readiness • Collaborate with Clinical Operations and regional teams to anticipate recruitment risks • Foster an inclusive, respectful team culture

🎯 Requirements

• Master’s or PhD in medical, pharma or biotech field strongly preferred; 12+ years in pharma/biotech required • Minimum of 5+ years leading cross-functional product teams within the pharma/biotech domain • Prior experience in oncology development and/or radiopharmaceuticals will be a distinct advantage • Experience in clinical Phase 2, Phase 3 and through approval required, specifically in the therapeutic area assigned • Demonstrated ability to think strategically, communicate effectively, and collaborate in a matrixed team environment • Direct people management experience is considered an advantage

🏖️ Benefits

• Competitive salaries • Annual performance-based bonuses • Equity-based incentive program • Generous vacation • Paid wellness days • Support for learning and development