Head Global Migraine​/Pain Pipeline, Medical Affairs; Senior Director​/Executive Medical Director

Job Description

The Medical Affairs organization provides patients, healthcare providers, and payers everywhere with the practical and clinically relevant information and solutions they need to use Abb Vie products safely and effectively, throughout the product lifecycle and the patient’s journey.

Purpose: Reporting to the Global Head of Neuroscience Pipeline, this role provides strategic medical and scientific leadership for core medical affairs activities in Abb Vie’s Migraine / Pain Pipeline Portfolio. This includes healthcare provider engagement strategies, critical data generation, educational initiatives, and patient safety. Key to success is partnering closely with commercial teams to influence product strategies, support market access, and drive scientific communications.

Offers medical insights and executes data generation, expert engagement, and communication initiatives across early and late‑stage development. Leads gap assessments, develops scientific communication platforms and wholistic value narrative (including clinical, societal & humanistic), and guides integrated evidence plans to enable launch readiness.

This position can be based from our Florham Park, NJ or Mettawa, IL sites and will follow a hybrid schedule of 3 days/week onsite.

• Advanced degree (MD/PhD/PharmD/DVM) required; post‑doctoral experience preferred.
• Senior Director requirements:
  Advanced degree with minimum 10 years’ experience in clinical trials or medical affairs (pharmaceutical industry or academia); typically 15 years overall experience.
• Executive Medical Director requirements: M.D. with minimum 5 years of clinical trial experience. 7+ years preferred.
• Strong leadership and cross‑functional team management skills in a global environment.
• Expertise in a relevant therapeutic area with ability to provide scientific strategy and support.
• Proven ability to independently lead clinical studies or medical affairs teams.
• Knowledge of clinical trial methodology, regulatory requirements, and protocol design.
• Excellent oral and written communication skills in English.
• People management experience preferred.

• Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law:
  The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range.
  
  This range may be modified in the future.
• We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.
• This job is eligible to…