Associate Medical Director – Renal Cancer Theranostics

This is a fully remote position, open to applicants in United States.

📋 Description

• Oversee the implementation of the medical affairs strategy for the renal cancer theranostic portfolio in the US.

• Play a key role in shaping medical strategy, setting priorities, formulating the medical operating plan, ensuring launch preparedness, and planning for the product lifecycle.

• Foster collaboration across Medical Affairs, Clinical Development, Commercial, Market Access, HEOR, Regulatory, Marketing, and Medical Information teams.

• Act as a subject-matter expert in renal cancer theranostics, providing scientific insights on evidence gaps and the competitive landscape.

• Offer medical leadership in reviewing clinical protocols, recruitment strategies, data interpretation, engaging investigators, managing expanded access programs, and evaluating investigator-initiated trial (IIT) protocols.

• Create and assess scientifically accurate medical materials, such as podium presentations, speaker decks, medical education initiatives, advisory board content, symposium resources, and both promotional and non-promotional materials through MLR review.

• Prepare and assist internal and external speakers effectively.

• Establish and nurture scientific relationships with key opinion leaders (KOLs), investigators, and professional organizations.

• Stay informed about recent publications, clinical trials, guidelines, patient journey dynamics, and competitive data, translating this knowledge into actionable recommendations for medical leadership.

⛳️ Requirements

• An advanced degree (PhD, PharmD, MD) with experience in renal oncology is required or an equivalent level of expertise.

• A minimum of 8 years of experience in Medical Affairs, including a background in leading cross-functional projects in oncology or specialty therapeutics.

• Familiarity with clinical operations, R&D, and/or medical affairs is essential.

• Preferred deep knowledge in renal cancer radiopharmaceuticals, theranostics, imaging and therapy integration, and the renal cancer patient journey.

• Experience in interpreting scientific data, market research, competitive intelligence, clinical utility evidence, and the evolving dynamics of clinical practice.

• Proficiency in the Microsoft Office Suite.

• Ability to contribute to medical strategy and lead cross-functional initiatives within a matrixed organization.

• Capability to engage with external and internal stakeholders to support the overall business strategy of the Company.

• Knowledge of clinical trial methodologies and regulatory requirements related to clinical trials, development strategies, and protocol design.

• Proven ability to collaborate effectively across matrixed teams and influence stakeholders without direct reporting authority.

• Excellent skills in verbal, written, and presentation communication.

• Capability to develop and implement medical affairs tactical plans that integrate lifecycle planning, competitive positioning, clinical utility, IIT, and support for clinical trial recruitment.

• Commitment to remaining updated with publications, clinical trials, congress data, and guideline revisions pertinent to renal cancer radiopharmaceuticals and theranostics.

• In-depth understanding of regulations and compliance standards related to industry interactions with healthcare professionals.

• Proven experience in building relationships with KOLs, investigators, and professional societies within the oncology field.

• A demonstrated history of achieving results that meet or surpass targeted objectives.

• A valid driver’s license is required.

🏝️ Benefits

• Competitive salaries.

• Annual performance-related bonuses.

• Equity-based incentive program.

• Generous vacation policy.

• Paid wellness days.

• Support for ongoing learning and development.

• An engaged and supportive team of colleagues.

• A global, interdisciplinary team environment.