[Hiring] Associate Medical Director @AMER

Role Description

The Associate Medical Director, Prostate Cancer Theranostics leads the execution of the US medical affairs plan across the prostate cancer theranostic portfolio, contributing to medical strategy, launch readiness, and lifecycle planning in partnership with the VP of Medical Affairs Americas. The role drives alignment of medical deliverables across various departments.

• Lead execution of the US medical affairs plan for the prostate cancer theranostic portfolio.
• Drive cross-functional alignment with US Medical Affairs, Clinical Development, Commercial, Market Access, HEOR, Regulatory, Marketing, and Medical Information.
• Contribute to medical affairs strategy for prostate cancer theranostic assets.
• Serve as a subject-matter expert on prostate cancer theranostics.
• Provide medical leadership on prostate cancer clinical protocol review.
• Develop and review scientifically accurate medical content.
• Prepare and support internal and external speakers.
• Build and maintain scientific relationships with KOLs, investigators, and professional societies.
• Maintain current knowledge of prostate cancer radiopharmaceutical publications and translate implications into recommendations.

Qualifications

• 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.
• Experience interpreting scientific data, market research, and competitive intelligence.
• Demonstrated ability to contribute to medical strategy and lead cross-functional execution.
• Excellent verbal, written, and presentation communication skills.
• Commitment to staying abreast of critical publications and guideline updates relevant to prostate cancer radiopharmaceuticals.
• Detailed knowledge of regulations and compliance practices related to industry interactions with healthcare professionals.
• Proven track record of delivering results that meet or exceed targeted objectives.
• Valid driver’s license.

Requirements

• Ability to interact externally and internally to support overall Company business strategy.
• Knowledge of clinical trial methodology and regulatory requirements governing clinical trials.
• Proven ability to collaborate effectively across matrixed teams and influence without direct reporting authority.
• Demonstrated ability to develop and execute medical affairs tactical plans.
• Experience building relationships with KOLs, investigators, and professional societies in oncology.

Benefits

• Commitment to excellence in work.
• Results-oriented approach to achieving goals.
• Encouragement of creativity and innovation.
• Strong communication skills across all levels.
• Collaboration as part of a team.
• Resilience in facing challenges.
• Inclusive mindset promoting diversity.
• Adaptability to dynamic environments.
• Commitment to ethical behavior.
• Focus on continuous learning and professional development.