Associate Medical Director, Prostate Cancer Theranostics

Telix Pharmaceuticals Limited

. Lead execution of the US medical affairs plan for the prostate cancer theranostic portfolio .

Posted 10/15/2026full-timeRemote • United StatesLeadWebsite

About the role

Key responsibilities & impact

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

Requirements

What you’ll need

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

Benefits

Comp & perks

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