Medical Director leading medical strategy for innovative evidence solutions in Neuroscience at Novartis. Managing complex assets and providing deep medical expertise across different disease areas.
Responsibilities
Lead development and execution of medical affairs strategy for TA/Asset priority programs including transformative tactics such as research/population health, innovative partnerships and integrated evidence plans
Co-develop plans for evidence generation, MSL / Field Medical Affairs strategy, medical education programs, scientific publication planning and Medical Expert network development with TAs
Co-own the development and implementation of 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
Partner with Development, S&G, US and International medical affairs, cross-functions to shape portfolio early and diversify evidence to achieve broad access at launch and to enhance impact on clinical practice for priority programs
Represent GMA around prioritized portfolio with internal and external audiences, in collaboration with TAs including the investment, medical and regulatory communities, as well as pharmaceutical or biotechnology industry collaborators/partners
Represent “the voice of the patient” internally and evaluate factors relevant to a patient’s informed decision making
Provide direction and input into the development and implementation of successful reimbursement and market-access strategies
Provide proactive input to Development on potential new therapeutic indications, to enrich Registration Programs and to consider new therapeutic opportunities.
Ensure that Patient Access programs are supported for all brands within the GMA and delivered with full compliance
Ensures GMA activities are designed and executed in compliance with company policy guidelines and highest medical quality standards
Provide proactive medical input to asset lifecycle management to consider new therapeutic opportunities.
Requirements
Must have: MD, Neurologist (Preferred) or PhD/PharmD in Neuroscience/ Health Sciences.
Specialist Degree or specialist qualification in Gene therapy related to discipline for which is responsible is an advantage
3+ years in Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development
Critical thinker and with ability to navigate uncertainty without major supervision
Fluent oral and written English; Other relevant languages are an advantage.
Strategic mindset and able to establish credibility and influence across a range of diverse stakeholders in a matrix organization to drive change
Ability to truly collaborate across functions and markets: serve-partner-co-create
Able to navigate in an environment of shared outcomes and cross-business accountabilities
Deep understanding of health care systems and key external stakeholders
Strong track record of delivery focus for time and quality in medical affairs projects
Successful development and implementation of innovative programs and processes
Understands unmet medical needs, generates the right evidence to fulfil them, uses innovative, multichannel communication formats for effective evidence dissemination
Credibility as peer expert with external stakeholders
Agile mindset & ability to lead in an agile organization across Disease Areas
Firm working knowledge of GCP, scientific and clinical methodology, protocol designs, management and regulatory requirements for clinical studies designated for review by regulatory authorities.
Benefits
Commitment to Diversity & Inclusion
Job title
Medical Director, Neuroscience – Global Medical Affairs
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