MI Subject Matter Expert (SME) for Local Considerations: • Provide support to Affiliate stakeholders to ensure MI activities comply with local regulatory requirements and organizational policies. Oversee the implementation of digital solutions to enhance MI capabilities and processes in the Affiliate. • Lead and implement local initiatives to integrate digital tools and platforms into MI operations, ensuring alignment with GMI goals. • Analyze data from medical inquiries to generate insights and develop analytical reports. • Present insights to regional and Affiliate stakeholders, providing trends and highlighting pertinent topics of interest. • Share Affiliate feedback on insights and escalated inquiries. • Serve as the contact for local business considerations, including Data Privacy, Pharmacovigilance, Regulatory Affairs, and other local regulations. Provide Data Privacy regulations to the Regional Medical Information database. Training and Forums: • Coordinate, facilitate and deliver MI training to the Affiliate team, as needed. • Collaborate with the Regional MI Team to update training materials regularly to reflect changes in processes, regulations, and GMI goals. • Actively participate in MI forums and Affiliate Medical Affairs/local Medical Operations meetings, sharing insights, best practices, and updates relevant to the Affiliate, regional and GMI landscape. Other Medical Operations Activities: • Manage other local Medical Operations responsibilities as needed and requested by the Medical Affairs/Operations leader(s). • Attention to detail and excellent analytical aptitude and clear, concise communication skills both verbally and in writing. • Researching, analyzing, and evaluating medical information materials using critical thinking skills and interpreting and applying medical information, instructions, policies and procedures and guidelines pertaining to medical communications and release of medical communications. • Familiarity with pharmaceutical principles, practices and their application, comprehension of medical terminology and treatment modalities and knowledge of pharmacology principles, theory and their application. • Capacity for driving process improvements and maintaining high-quality standards. • Experience in leading cross-regional initiatives and coordinating between diverse teams. • Sensitivity to cultural differences and an awareness of differences in medical and clinical practice in the region. • Fluency in English and an appreciation of the difficulties and ambiguities in English language usage in the region. • Knowledge and experience in use of computer systems and database and software applications, including Microsoft Office, Power Point, and Excel preferred.

Minimum of B.S. degree with an emphasis in Science, Health Care or related fields from an accredited college or university. Advanced degrees (MSc/PharmD/PhD) would be preferred, and/or 2+ years of pharmaceutical industry experience (MI experience preferred) or 4+ years of health care related field experience. • Working knowledge of current regulatory requirements (e.g. European Medicines, Pharmaceutical and Devices Agency, Food and Drug Administration), and/or other guidelines and knowledge of AbbVie therapeutic areas and research interests desired.
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