Tedi Soule
PharmD | Oncology Medical Affairs | Educator | Lifelong Learner
- Role
- Global Medical Strategy Lead, Oncology at GSK
- Location
- Raleigh, NC, US
- LinkedIn followers
- 500 followers
About Tedi Soule
Accomplished medical affairs leader with over 15 years of experience delivering strategic impact across the U.S. and global healthcare landscapes. My career spans medical strategy, scientific communications, stakeholder engagement, and clinical development, anchored in a deep commitment to translating complex science into meaningful and actionable insights.Throughout my journey, I have led and supported successful product launches, shaped brand evidence generation strategies, and pioneered innovative educational platforms. I am proud to have mentored high-performing future leaders known for their agility, scientific rigor, and collaborative mindset.My ability to bridge science with strategic vision has made me a trusted partner to cross-functional teams and external stakeholders alike. Whether it\'s enhancing scientific alignment across the product life cycle or generating data-driven insights to inform decision-making, I bring precision, purpose and passion to every initiative.I thrive at the intersection of science, strategy, and storytelling, and am always looking to connect with forward-thinking professionals committed to advancing patient care and elevating the role of medical affairs in today\'s evolving healthcare ecosystem.Let\'s connect!
Experience
Global Medical Strategy Lead, Oncology
Nov 2022 — Present · Raleigh-Durham-Chapel Hill, NC, US
As a Global Medical Affairs Lead - Oncology at GSK, I have had the privilege of steering global medical affairs strategy for multiple oncology pipeline assets with complex development programs across multiple tumor types at critical stages of their development. This role has demanded not just scientific acumen, but strategic foresight, cross-functional leadership, and the ability to translate complex data into clear, compelling narratives that inform decisions and accelerate progress.Partnering with world-class researchers, regulators, and internal stakeholders, I drive alignment between scientific integrity, regulatory applications, and commercial vision- ensuring that every step we take is grounded in purpose and precision. Whether leading study task forces to accelerate trial enrollment or crafting training that elevates scientific fluency across teams, I aim to make an impact that advances not just assets, but outcomes for patients.Key contributions:• Skilled at developing new relationships and actively engaging with top scientific experts worldwide to derive actionable insights that directly shape clinical development strategy, refine clinical trial design, and inform medical affairs evidence generation plans that strengthen therapeutic value and address unmet needs • Orchestrate impactful scientific communications by shaping global publication strategies, data dissemination plans, and medical education content• Influence asset positioning by delivering medical oversight for regulatory submissions and health authority interactions• Experience in navigating the complexities of Alliance partnerships and establishing effective ways of working that align stakeholders, build trust, and drive Medical Affairs strategies forward
Education
Albany College of Pharmacy and Health Sciences
Doctor of Pharmacy (Pharm.D.)
The University of North Carolina at Chapel Hill
Drug Development and Clinical Research Fellowship
2007 — 2008
University of Maryland School of Pharmacy
Comparative Effectiveness Research in Decision Making Certificate Program
2017
Skills
- Infectious Diseases
- Regulatory Affairs
- Pharmaceutical Industry
- Oncology
- Medical Writing
- Clinical Trials
- Clinical Research
- Clinical Development
- Drug Development
- Gcp
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