Global Medical Director – Cell & Gene Therapy (Oncology)
Location : London, UK, Dublin, Ireland or Barcelona, Spain | Role Type : Hybrid Working
We are looking for a Global Medical Director to lead medical strategy for Cell & Gene Therapy (C>
) Oncology across the global asset lifecycle. The role focuses on innovative evidence solutions including interventional studies, Non-Interventional Studies (NIS) and Real World Evidence (RWE) studies and implementation science projects.
Major Accountabilities
- Lead medical affairs strategy and execution for Oncology C>
priority programs, including research, innovative partnerships and integrated evidence plans.
Co-develop evidence generation plans, MSL / Field Medical Affairs strategy, medical education, scientific publication planning and Medical Expert network development.Co-own innovative education and scientific communication plans for external stakeholders.Financial tracking to ensure timely and cost-effective development & execution of medical activities.Prepare Scientific Review Committee submissions for TA assets within remit.Partner with Development, Strategy and Growth (S&G), US and International cross-functions to shape portfolio early and diversify evidence to achieve broad access at launch.Represent GMA around prioritized portfolio with internal and external audiences, collaborating with TAs.Represent “the voice of the patient” internally and evaluate factors relevant to patient decision‑making.Other Duties
Provide direction on reimbursement and market‑access strategies.Provide proactive input to Development on new therapeutic indications.Ensure Patient Access programs are supported and compliant.Ensure GMA activities comply with company policy and medical quality standards.Provide medical input to asset lifecycle management to consider new therapeutic opportunities.Essential Requirements
MD (Preferred) or PhD / PharmD in Health Sciences. Specialist qualification related to discipline is an advantage.5+ years in Pharmaceutical Industry experience in Medical Affairs and / or Clinical Development.Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies.Strategic mindset with ability to influence across diverse stakeholders in a matrix organization.Deep understanding of healthcare systems and key external stakeholders.Strong track record of delivery focus in medical affairs projects.Understands unmet medical needs, generates the right evidence and uses innovative communication formats.Highly Preferred
Cell & Gene expertise with experience in early asset lifecycle, pre‑launch and launch in Global organizations.Experience in developing and executing “Best in Class” processes at scale.Clinical trial research experience in a pharmaceutical or equivalent academic environment.Why Novartis
Our purpose is to reimagine medicine to improve and extend people’s lives. Join us to help create breakthrough therapies for patients worldwide.
Benefits and Rewards
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