Clinical Research Associate (CRA, klinischer Monitor)

7/2016 – offen

Supervision of phase I, III and IV studies in the field of breast and renal cell cancer encompassing site selection visits, review of protocol information with investigators, collection of documents for ethics submission and assuring site readyness, site initiation, onsite and remote monitoring and close-out visits including CRF review and Source Data Verification, drug accountability, maintenance of TMF and ISF by reviewing and archiving critical documents according to ICH-GCP, German drug law, other applicable regulations and SOPs.

Klinische Studie, Klinische Monitor (CRA)