Medical Asset Lead Director, Oncology
Based in the United StatesFull-TimeDirector
Salary$217,673.10 to $294,498.90 USD
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Job Details
- Required Skills
- Stakeholder management
Requirements
- Doctorate, Master's, or Bachelor's degree with significant progressive experience in medical affairs or clinical development within a relevant therapeutic area.
- MD, DO, PharmD, or PhD preferred, with advanced clinical training or board certification considered a strong advantage.
- Extensive leadership experience within the biotechnology, pharmaceutical, or CRO industry, including managing global or cross-functional medical affairs initiatives.
- Strong expertise in oncology, including experience with hematologic malignancies and evolving treatment landscapes.
- Proven ability to develop and execute integrated evidence generation strategies and global medical affairs plans.
- Strong understanding of pharmaceutical development, commercialization, global regulatory requirements, Good Clinical Practice (GCP), and healthcare systems.
- Demonstrated success leading matrixed teams, influencing senior stakeholders, and collaborating across global organizations.
- Excellent strategic thinking, scientific communication, stakeholder engagement, leadership, and decision-making skills with the ability to translate complex data into actionable medical strategies.
Responsibilities
- Lead the development and execution of global medical affairs strategies for oncology assets across marketed products, lifecycle management initiatives, and pipeline programs.
- Provide leadership, coaching, and development for a high-performing global medical affairs team while supporting organizational growth and succession planning.
- Partner with cross-functional and regional teams to align medical strategies with clinical development, commercial priorities, evidence generation, and product lifecycle plans.
- Guide integrated evidence generation initiatives, scientific communications, publication strategies, advisory boards, congress activities, and stakeholder engagement plans.
- Build strong relationships with healthcare professionals, key opinion leaders, advocacy organizations, payers, regulators, and other external stakeholders to gather insights and strengthen scientific collaboration.
- Contribute medical expertise to target product profiles, clinical development plans, value dossiers, and benefit-risk assessments.
- Oversee medical affairs studies, budget planning, resource allocation, and operational execution while ensuring compliance with applicable regulations and industry standards.
- Monitor performance metrics, identify opportunities for continuous improvement, and drive excellence across global medical affairs activities.
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