Head Global Migraine/Pain Pipeline, Medical Affairs (Senior Director/Executive Medical Director)

Responsibilities

• Lead, oversee, and support assigned indications and projects in collaboration with cross-functional teams (Medical, Clinical Development, Commercial, Market Access, HEOR).
• Initiate and manage medical affairs activities, data generation, and dissemination to advance scientific and business objectives.
• Provide scientific and technical support for assets, deliver presentations, maintain relationships with key opinion leaders, and contribute to cross-functional teams.
• Guide development of Target Product Profiles (TPP), contribute to Phase II-III trial design, and lead Phase 3b/4 strategies in alignment with TPP.
• Lead the planning and execution of advisory boards, scientific, and medical education programs for both internal and external stakeholders.
• Stay current on scientific advancements and literature; act as a resource for Migraine and Pain therapeutic areas. Initiate and publish research projects.
• Lead cross-functional teams on discrete projects such as data analysis, expert engagement, publications, and collaborations.
• Represent Medical Affairs in due diligence activities for asset acquisitions aligned with disease area strategy.
• Ensure scientific initiatives meet budget, timeline, and compliance requirements.
• Manages a team of high performing colleagues.
• 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:
• 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 participate in our long-term incentive programs.
• AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.
• US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html
• US & Puerto Rico applicant

Benefits

Additional Information

The Medical Affairs organization provides patients, healthcare providers, and payers everywhere with the practical and clinically relevant information and solutions they need to use AbbVie 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 AbbVie'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.

Your Match

How well this role fits your profile.

Company Intel

What employees say

Worked at Abbvie? Share your experience