Mr. Sascha Seidl
Sascha Seidl started his Clinical Research career in the clinical operations group of a small CRO over 10 years ago. He currently holds the position “Associate Director Clinical Trial Transparency” at Merck KGaA, Darmstadt, Germany. Sascha currently manages Merck’s “Responsible Data Sharing” activities and developed several Merck Quality Documents and Processes for various clinical trial data disclosure deliverables. He is a member of the TransCelerate Placebo and Standard of Care initiative and participated in all EMA EU Portal User Acceptance Testings. Sascha holds a MSc degree in Biology from University of Muenster and is a certified Clinical Research Associate/Clinical Data Manager from mibeg Institut Medizin, Cologne, and a Lean & Six Sigma green belt.