Executive Medical Director

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 X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok.

Job Description

Job Description

The Executive Medical Director is responsible for the safety strategy for solid tumors late-stage oncology portfolio, and to supervise, manage and mentor the safety physicians (Group MDs, Senior MDs and medical directors) and supporting the Solid Tumor in the Oncology TA. The Executive Medical Director will be the oncology safety team connector across R&D, will promote forward thinking safety strategy for the oncology platform in late stage.

Responsibilities:

• Set safety strategy for the solid tumors late-stage portfolio considering AbbVie Oncology priorities.
• Help Develop the strategy for a personalized safety approach trough collaboration with internal partners such as precision medicine.
• Safety representative for cross-functional teams across assets and the counterpart to the Executive Medical Director for the product/portfolio on the Clinical Team.
• Overarching experts in solid tumors space including in depth understanding of SOC, disease characterization based on biomarkers and line of treatments.
• Keeping the solid tumors knowledge up to date (up to date on NCCN, ASCO, ASH, EHA and ESMO guidelines, targeted conference attendance) including understanding of competitive intelligence and emerging internal data (clinical and beyond)
• Managing and mentoring Group Medical director/s and Product Safety Team Leads and other safety colleagues within Oncology/Solid tumor area.
• Interacts with and influences other cross functional departments (e.g. Clinical Development, Regulatory Affairs, Medical Affairs), as needed, to ensure the successful development, design, and implementation of comprehensive safety assessment to