Mike Pacak

Mike Pacak is an experienced management professional specializing in pharmaceutical GCP, GMP, and GLP Quality Assurance compliance, Quality Control, and Drug Safety. Currently serving as Associate Director of Clinical Quality Assurance at Alkermes since March 2018, Mike has held various senior roles across multiple organizations, including Associate Director at Karyopharm Therapeutics Inc. and Principal Consultant at Highridge Pharma Consulting. With a solid educational background, including an MBA from Kent State University and a Master's in Biology from Youngstown State University, Mike has a proven track record in ensuring compliance with industry regulations, conducting audits, and supporting clinical and non-clinical activities in drug development, particularly in oncology.