Clinical Research Associate (CRA)

The CRA has responsibility for the delivery of the studies at allocated sites and are active participants in the study team(s). The CRA works in close collaboration with other CRAs and the Study Team to ensure that quality and quantity commitments are achieved in a timely and efficient manner. The CRA is responsible for the preparation, initiation, monitoring and closure of an agreed number of sites in clinical studies according to Laekna Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations. Deliver according to the commitment in the individual trials.