Timm joined PharmaLex in 2014 as Head of Global Regulatory Operations. He is responsible for all world-wide electronic submission activities, regulatory information management and related topics. He is also leading and supporting process optimization projects within Regulatory Affairs as well as providing consultancy for Regulatory Information Management, IDMP-related topics, as well as for eCTD publishing and other Regulatory systems. Since 2021 Timm is also responsible for driving the R&D Informatics strategy at PharmaLex, streamlining software systems and technologies across PharmaLex’ service solutions.
Timm has about 20 years of experience within Pharma R&D and about 15 years of experience within Regulatory Affairs. Previously he worked at Merck Serono heading the Dossier & Submission Management department and at Baxter, where he held several global positions in Biostatistics, Pharmacovigilance and R&D IT. He is a notable speaker and session chair at international conferences and seminars.
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