Clinical Monitor | Klinischer Monitor (m/w/d)

Job Summary

The Center for Clinical Studies is seeking a dedicated and competent Clinical Monitor to join their team, focusing on investigator-initiated clinical trials across various therapeutic areas. This role offers a diverse range of responsibilities, including preparing, conducting, and documenting monitoring visits at study sites nationwide. You will be responsible for site support, training, developing risk-based monitoring concepts, and contributing to essential study documents and internal SOPs. The position is attractive due to its scientifically oriented nature, challenging tasks, and the opportunity to work within a supportive, multidisciplinary team in a promotion-oriented environment. Key requirements include a life sciences degree or medical vocational training with CRA experience, strong knowledge of GCP and relevant legislation, and excellent English and German language skills.