
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.
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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.
• Lead execution of the US medical affairs plan for the prostate cancer theranostic portfolio • Contribute to medical strategy, priorities, medical operating plan, launch readiness, and lifecycle planning • Drive cross-functional alignment across US Medical Affairs, Clinical Development, Commercial, Market Access, HEOR, Regulatory, Marketing, and Medical Information • Serve as subject-matter expert on prostate cancer theranostics and provide scientific input into medical planning, evidence gaps, and competitive landscape • Provide medical leadership on clinical protocol review, recruitment strategy, data interpretation, investigator engagement, expanded access programs, clinical registries, and IIT protocol review • Develop and review scientifically accurate medical content, including podium materials, speaker decks, medical education programs, advisory board content, symposia materials, and promotional/non-promotional resources through MLR review • Prepare and support internal and external speakers • Build and maintain scientific relationships with KOLs, investigators, and professional societies • Maintain current knowledge of publications, clinical trials, treatment guidelines, patient journey dynamics, and competitive data • Translate emerging scientific data and implications into recommendations for medical leadership
• Advanced degree (PhD, PharmD, MD) with prostate oncology experience required or equivalent experience • 8+ years of Medical Affairs experience, including experience leading cross-functional initiatives in oncology or specialty therapeutics • Experience working with clinical operations, R&D and/or medical affairs • Deep expertise in prostate cancer radiopharmaceuticals, theranostics, imaging and therapy integration, and the prostate cancer patient journey preferred • Experience interpreting scientific data, market research, competitive intelligence, clinical utility evidence, and evolving clinical practice dynamics • Proficient in Microsoft Office Suite • Demonstrated ability to contribute to medical strategy and lead cross-functional execution in a matrixed environment • Ability to interact externally and internally to support overall Company business strategy • Knowledge of clinical trial methodology and regulatory requirements governing clinical trials • Experience in development strategy and protocol design • Proven ability to collaborate effectively across matrixed teams and influence without direct reporting authority • Excellent verbal, written, and presentation communication skills • Ability to develop medical content for scientific exchange, speaker preparation, and podium presentations • Ability to develop and execute medical affairs tactical plans incorporating lifecycle planning, competitive positioning, clinical utility, IIT, and clinical trial recruitment support • Commitment to staying abreast of critical publications, clinical trials, congress data, and guideline updates relevant to prostate cancer radiopharmaceuticals and theranostics • Detailed knowledge of regulations and compliance practices related to industry interactions with healthcare professionals • Experience building relationships with KOLs, investigators, and professional societies in oncology • Proven track record of delivering results that meet or exceed targeted objectives • Valid driver’s license
• Competitive salaries • Annual performance-based bonuses • Equity-based incentive program • Generous vacation • Paid wellness days • Support for learning and development • Supportive group of colleagues • Global, interdisciplinary team environment
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