At least five years of experience in clinical research within an international environment, including a minimum of three years in clinical site monitoring - To enlarge our Clinical Programs EMEA team we are looking as soon as possible for a * Actively participating in the creation of clinical monitoring plans, monitoring tools, visit report annotations, and CRA training materials, you also promote the ongoing enhancement of monitoring SOPs and templates to make monitoring activities more efficient and intelligent * Conducting co-monitoring visits internationally or, if necessary, on-site visits in the DACH region, including SQV, SIVs, IMVs or COVs, to guarantee consistency, quality, and strong relationships with our clinical sites throughout * Phenox GmbH * Bochum, eu
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