Medical Director/Scientific Director, Medical Affairs - Precision Medicine

Company Description

AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on Twitter, Facebook, Instagram, YouTube and LinkedIn. 

Job Description

*Preferred location is Lake County, IL (hybrid 3 days per week). Will consider remote candidates. 

*Position title will be based on qualifications listed below.

Purpose

• Global Medical Affairs (GMA) leader accountable for the creation and oversight of the execution of our Companion Diagnostics (CDx) Global Medical Affairs (GMA) objectives.
• Oversees GMA CDx activities ensuring seamless communication and execution on Oncology early CDx launch strategies.
• Provide strategic support to and guidance to the therapeutic area team in developing, aligning, and executing our early CDx strategies with our Oncology pipeline assets strategies.

Responsibilities

• Develop and coordinate the overarching CDx strategy across multiple early oncology assets to ensure optimal launch planning of our assets.
• Lead the development and implementation of diagnostic strategies for individual assets.
• Serve as a key member and content expert in the Pipeline Commercialization Model.  Serve as a key member of the Asset Strategy Teams and Integrated Evidence Teams to shape the development and early launch planning of our companion diagnostics for various assets and indications across the oncology pipeline.
• Build together with clinical development and precision medicine a comprehensive plan to address the evidence, educational, and standard of care gaps and ensure GMA input into the CDx development strategies. 
  • Responsible for understanding the different regulatory requirements across the geographical areas related to clinical studies and accountable for complying with those requirements.
  • May assist with the scientific review, development, e