All ourmulti-lingualSenior CRAs are self-employed and therefore highly motivated and organised, with at least four years of solid field-based experience. Without exception, all have considerable experience in feasibility,EC & CA submissions, site management and monitoring of clinical Phase I-IV, observational and medical device trials across a wide range of therapeutic areas. ICH GCP guidelines are strictly adhered to. Excellent contacts with Ethics Committees and Regulatory Authorities expedite study set-ups.
Geographical areas
Our Pan-European network can provide your project
with Senior CRAs and verified protocol translators. We have supported the start-up of many freelancers.
Contracting local CRAs means less travel
costs, in-depth knowledge of local regulatory
requirements and good cultural awareness.
