Immedica Pharma AB
Margit Pelcman is a seasoned professional in the field of regulatory operations and clinical development, currently serving as the Senior Manager of Global Regulatory Operations at Immedica Pharma AB since August 2025. Prior to this role, Margit Pelcman spent eight years at Sobi - Swedish Orphan Biovitrum AB (publ) as the Global Regulatory Operations Manager, following an extensive tenure at the same organization in various positions including Clinical Study Manager and Clinical Data and Documentation Manager. Margit Pelcman's career began at Biovitrum AB, where responsibilities included Clinical Trial Associate and Development Chemist, complemented by earlier experience at Pharmacia as a Development Chemist. Margit Pelcman holds a Master of Science in Chemical Engineering from KTH Royal Institute of Technology, earned between 1988 and 1994.
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