Telix Pharmaceuticals Limited · 12 hours ago
Global Product Development Lead – TLX090
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Biotechnology
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Responsibilities
Leads technical cross-functional team to achieve milestones and advance through stage-gates.
Champion the development of late-stage radiopharmaceutical compounds, ensuring alignment with company strategy and objectives.
Contribute to clinical trial strategy, gathering input from stakeholders and providing expertise.
Create integrated development plan encompassing timelines for all functions.
Overcome obstacles to ensure programs progress in a timely manner.
Showcase prowess in strategic thinking, particularly in the realm of cross-functional drug development, guiding matrixed teams through complex decision-making and risk management processes.
Co-lead and create strategic direction with Global Commercial Lead.
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 to formulate plans that achieve program milestones and objectives.
Partner with Clinical and Regulatory Affairs to craft the ideal development pathway for approval, aiming to meet product attributes and commercial objectives.
Assume accountability for reporting the progression of assigned drug development program, presenting data through dashboards and management reviews.
Create and execute comprehensive product development plans and data packages, paving the way for informed go/no-go decisions and continuous progression towards product approval.
Engage subject matter experts and thought leaders, both within and outside the organization, fostering rich scientific dialogue, extracting insights, and refining development plans and strategies.
Excellent team management skills required.
Lead team and manage conflicting views diverging views on team, and spearhead team towards solutions and progress.
Liaise with senior management for input and updating programs.
Excellent presentation skills and executive presence required.
Lead development, regulatory, CMC, clinical operations, manufacturing through preparations for submitting regulatory filings and ultimately product launch.
Qualification
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Required
Master’s or PhD strongly preferred; bachelor’s degree with minimum 10+ years considered in lieu of advanced degree.
10+ years leading cross-functional product teams within the pharma/biotech domain required.
Prior experience in oncology development and/or radiopharmaceuticals will be a distinct advantage.
Experience in clinical Phase 2 through approval required, specifically in the musculoskeletal therapeutic area strongly preferred.
Demonstrated ability to think strategically, communicate effectively, and collaborate in a matrixed team environment.
Excellent team management skills required.
Excellent presentation skills and executive presence required.
Preferred
Experience in clinical Phase 2 through approval specifically in the musculoskeletal therapeutic area strongly preferred.
Benefits
Competitive salaries
Annual performance-based bonuses
An equity-based incentive program
Generous vacation
Paid wellness days
Support for learning and development
Company
Telix Pharmaceuticals Limited
Telix is a biopharmaceutical company focused on the development and commercialisation of therapeutic and diagnostic ('theranostic') radiopharmaceuticals.
Funding
Current Stage
Public CompanyTotal Funding
$494.87MKey Investors
Australian Government
2024-11-13IPO
2024-07-23Post Ipo Debt· $431.37M
2022-04-04Grant· $23M
Leadership Team
Recent News
2024-12-02
BioWorld Financial Watch
2024-11-24
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