Hybrid Associate Director, Global Medical Affairs – Renal

at Novartis

• Job title: Associate Director, Global Medical Affairs – Renal
• Job type: Full Time
• Experience level: Senior
• Salary: Not specified
• Degree requirement: Postgraduate Degree
• Tech skills: Google Cloud Platform
• Location requirements: Hybrid, Barcelona, Spain

About the role

• Associate Director leading medical affairs strategy for global renal programs in a pharmaceutical company. Focusing on evidence generation and partnerships to enhance patient access and impact clinical practice.

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 SRC submissions for TA assets within remit
• Partner with Development, S&G, US and International 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
• Ensure that Patient Access programs are supported by all brands within International Medical Affairs and delivered with full compliance

Requirements

• Must have: MD (Nephrologist Preferred) or PhD/PharmD in Health Sciences. Specialist Degree or specialist qualification related to discipline for which you will be responsible is an advantage.
• 5+ years of Pharmaceutical Industry experience in Medical Affairs and/or Clinical Development, preferable in renal diseases
• 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 like nephrologists and nephropathologists
• Strong track record of delivery focus for time and quality in medical affairs projects, i.e. advisory board, publications, study development
• 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: Novartis is committed to building an outstanding, inclusive work environment and diverse teams representative of the patients and communities we serve.