VP, Clinical Science

🕒 February 19

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Logo of Telix Pharmaceuticals Limited

Telix Pharmaceuticals Limited

501 - 1000 employees

Founded 2015

🧬 Biotechnology

💊 Pharmaceuticals

⚕️ Healthcare Insurance

Biotechnology • Pharmaceuticals • Healthcare Insurance

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

• Support the design, strategy, and operationalization of clinical trials during the drug development process from Phase 0 to Phase 4 • Develop study documentation including study protocols, investigators brochures, informed consent documents, clinical dossiers for regulatory submissions • Provide scientific input into documentation including investigators brochures, investigational medicinal product dossiers, developmental safety update reports and clinical study reports • Review study data including safety and efficacy data for accuracy and quality • Triage and delegate work requests to the in-house team of subject matter experts • Work closely with Clinical Operations, Medical Affairs, and asset matrix teams to ensure compliance with organizational SOPs • Assist in development and participate as needed, in Steering Committees and Advisory Boards with global thought leaders • Provide senior management personnel regular updates on the progress of the clinical research • Review imaging studies and be qualified to provide input on interpretation, quality assurance, accuracy of imaging interpretation, and final review of imaging, protocols, and imaging charters prior to implementation • Coordinate efforts associated with clinical imaging, pharmacology, biostatistics, and physics subject matter experts to address complex trial related questions/strategy

🎯 Requirements

• Scientific background with university degree and MD required • 10+ years Clinical experience with strong sponsor or CRO experience required • 5+ years’ experience leading teams required • Detailed knowledge of global clinical trial regulations • Formal training in clinical diagnostic imaging (e.g. Radiology, Nuclear Medicine, Radiation Oncology) with Clinical Fellowship level training in Oncology associated field • Familiarity with managing groups within matrix teams

🏖️ Benefits

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

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