AbbVie - Mettawa, IL

posted 5 months ago

Full-time - Senior
Hybrid - Mettawa, IL
1,001-5,000 employees
Chemical Manufacturing

About the position

The Scientific Director for Medical Affairs in GI Care for exocrine pancreatic insufficiency (EPI) at AbbVie is responsible for providing strategic and operational input into core medical affairs activities. This includes evidence generation through clinical trials, stakeholder interactions, educational initiatives, and scientific communications. The role involves collaboration with various functional areas to drive innovation and life cycle management of medicines, ensuring comprehensive medical strategies are developed and executed effectively.

Responsibilities

  • Provide leadership, oversight, and support for assigned indications/projects in collaboration with Clinical Development, Commercial, Market Access, HEOR, and other functional areas.
  • Work closely with Brand Teams and relevant cross-functional teams to provide strategic input into core scientific strategy and drive Medical Affairs activities.
  • Lead or provide input into the design, analysis, interpretation, and reporting of scientific and medical data across study protocols and regulatory submissions.
  • Oversee Medical Affairs-led clinical studies, monitoring overall study integrity and communication of accumulating data pertaining to safety and efficacy.
  • Develop and maintain professional relationships with key opinion leaders and participate in cross-functional teams to ensure broad perspectives are incorporated into Clinical Development Plans.
  • Assist in the development of scientifically accurate marketing materials, medical education programs, and advisory boards.
  • Ensure projects are completed on time, on budget, and in compliance with AbbVie's policies and regulatory requirements.

Requirements

  • Advanced Degree (PhD, NP/PA, or PharmD) with additional post doctorate experience preferred.
  • Typically, 10+ years of experience in the pharmaceutical industry or equivalent.
  • Minimum of 4 years of clinical trials or research management experience in the pharmaceutical industry or academia preferred.
  • Knowledge of clinical trial methodology, data analysis and interpretation, and regulatory requirements governing clinical trials.
  • Proven leadership skills in a cross-functional team environment.
  • Excellent oral and written English communication skills.

Nice-to-haves

  • Experience in medical affairs within the pharmaceutical industry.
  • Familiarity with evidence generation and scientific communications.

Benefits

  • 401(k)
  • Dental insurance
  • Health insurance
  • Paid holidays
  • Paid time off
  • Vision insurance
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