Strategic Medical Affairs Director

AbbVie Inc.; Mettawa (IL); On-site; USD 180,000 - 260,000; Full time

Job summary

AbbVie Inc. is seeking a Scientific Director to provide medical and scientific input into medical affairs activities, education initiatives, and risk management.

You will work with commercial teams to support product strategies, launches, and market access, while collaborating with clinical development on priority trials. You will lead Medical Affairs initiatives for the indicated area, develop education programs, plan advisory boards, and ensure timely reviews of promotional materials in

Qualifications

• Advanced degree and relevant pharmaceutical experience.
• 5-7+ years in the pharmaceutical industry or equivalent.
• Knowledge of clinical trial methodology and regulatory requirements.
• Ability to present technical information to varied audiences.
• Excellent oral and written communication with internal and external stakeholders.
• Coordinate scientific and medical activities across teams.

Responsibilities

• Contributes to development of brand strategies and engagement plans.
• Leads and supports Medical Affairs initiatives for target indications.
• Develops Medical Education / Advisory Boards and conference planning.
• Generates clinical and scientific data per evidence gap assessment.
• Manages budgets for assigned projects.
• Aligns education and initiatives with Scientific Communication Platform.
• Supports IIS strategy and investigator initiated studies.
• Reviews medical advertising materials for accuracy and regulatory compliance.
• Supports safety and risk management plans and reviews.

Skills

Oral and written communication

Stakeholder management

Presentation skills

Regulatory understanding

Education

Advanced degree (PhD, PharmD, PA or NP)

Job description

AbbVie Inc. is seeking a Scientific Director to provide medical and scientific input into medical affairs activities, education initiatives, and risk management.

You will work with commercial teams to support product strategies, launches, and market access, while collaborating with clinical development on priority trials. You will lead Medical Affairs initiatives for the indicated area, develop education programs, plan advisory boards, and ensure timely reviews of promotional materials in