Company Description Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Lead Start up Specialist in Germany with fluent German. Job Overview Responsible for CA & Ethics Committee (EC) submission Keep up to date knowledge of GCP and ICH Guidelines for clinical research. Translation and co-ordination of translations for documents required for submissions. Supervising study conduct according to GCP requirements and all applicable laws. Key Requirements Bachelor degree in life-science Min 1 year in EC & CA submissions within a CRO, Pharma, Biotech in Germany Experience in clinical studies phase II-III Fluent English & German Excellent communication skills FTE: 1.0 #J-18808-Ljbffr