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Associate Medical Director – Renal Cancer Theranostics
Telix Pharmaceuticals Limited. Lead execution of the US medical affairs plan for the renal cancer theranostic portfolio .
About the role
Key responsibilities & impact- Lead execution of the US medical affairs plan for the renal cancer theranostic portfolio
- Contribute to medical strategy, priorities, medical operating plan, launch readiness, and lifecycle planning
- Drive cross-functional alignment across Medical Affairs, Clinical Development, Commercial, Market Access, HEOR, Regulatory, Marketing, and Medical Information
- Serve as subject-matter expert on renal cancer theranostics and provide scientific input on 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, guidelines, patient journey dynamics, and competitive data, translating implications into recommendations for medical leadership
Requirements
What you’ll need- Advanced degree (PhD, PharmD, MD) with renal 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 renal cancer radiopharmaceuticals, theranostics, imaging and therapy integration, and the renal cancer patient journey preferred
- Experience interpreting scientific data, market research, competitive intelligence, clinical utility evidence, and evolving clinical practice dynamics
- Proficiency in Microsoft Office Suite
- 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, regulatory requirements governing clinical trials, development strategy, and protocol design
- Ability to collaborate effectively across matrixed teams and influence without direct reporting authority
- Excellent verbal, written, and presentation communication skills
- 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 current with publications, clinical trials, congress data, and guideline updates relevant to renal 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 meeting or exceeding targeted objectives
- Valid driver’s license
Benefits
Comp & perks- Competitive salaries
- Annual performance-based bonuses
- Equity-based incentive program
- Generous vacation
- Paid wellness days
- Support for learning and development
- Engaged and supportive group of colleagues
- Global, interdisciplinary team environment