Descripción de la oferta
Experteer Overview
As Global Medical Lead in Ferrer’s Neurology Therapeutical Area, you drive the Global Medical Strategy and the Integrated Evidence Generation Plan for your products. You align medical leadership with corporate strategy and collaborate with internal teams, affiliates, and external scientific partners to shape the value proposition and launch readiness. You will oversee medical communications and publications, ensuring scientifically sound materials and engagement with key stakeholders. This role offers meaningful impact in shaping medical strategy across a global organization and advancing patient care.
Compensaciones / Beneficios
• Lead the Global Medical Affairs Strategy and Tactical plan for strategic products
• Lead Integrated Evidence Generation Plan (IEGP) for strategic products
• Interpret key scientific data and identify unmet medical and educational needs
• Critically evaluate disease areas, competitive landscape, and synthesize data to support brand strategy and development
• Scientifically lead and co-lead launch readiness for assets in development with cross-functional coordination
• Drive development of medical education messages and materials using insights and launch strategies
• Drive medical and scientific communication alignment with Scientific Communications
• Design and align the Global Product Publication Plan
• Develop training strategy and content with Scientific Training
• Provide medical evaluation and approval for promotional/educational materials
• Lead scientific communication engagement strategy
• Develop external relationships with medical groups, societies, and stakeholders
• Central point of contact for Medical roles in Affiliates/Partners to ensure collaboration
• Maintain close working relationship with Sales, Marketing, Market Access, Patient Advocacy, Regulatory, Ru0026D
Responsabilidades
• 5+ years as Medical Affairs Advisor or Lead
• Therapeutic area experience in Neurology and/or rare/orphan conditions
• Proven track record leading cross-business/cross-functional planning
• Solid peer relationships with external experts, regulatory bodies, pharma associations
• Regional or global experience is a plus
• Contributions to medical strategies and launches are a plus
• Strong understanding of clinical development and real-world evidence plans
• Familiar with GCP and promotional material regulations
• Knowledge of clinical trial design, statistics, and pharmacokinetics
• Familiar with marketing principles and medical writing
• Languages: fluent in English and Spanish
Requisitos principales
• volunteering opportunities
• flexible working model
• collaborative office environment
• development and learning opportunities
• remuneration and benefits customization
• wellbeing support
