Matt Robillard is a Senior Director at AbbVie, where they lead the Regulatory Strategic Writing group, providing critical medical writing support for clinical development. With 25 years of extensive experience in global drug development, Matt previously served as a Director at PRA Health Sciences, managing clinical development submissions across various therapeutic areas. Their background includes roles at Abbott, Takeda Global Research & Development Center, and Takeda Pharmaceuticals, emphasizing their expertise in strategic communication within multi-disciplinary projects. Matt earned a Master of Business Administration (M.B.A.) in Organizational Leadership from Lake Forest Graduate School of Management.
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