Clinical Research Associate Location: Belfast / requires travel when required Job Purpose: Act in the role of clinical site monitor to regularly visit/remotely assess in vitro diagnostic medical device clinical study sites and ensure that the study is conducted in compliance with the study protocol, ICH GCP and local regulatory requirements.
Interested in this role You can find all the relevant information in the description below.
Key Responsibilities: The CRA will be involved in all aspectsof the in vitro diagnostic clinical trial, including qualification of investigational sites as well as setting up, initiating, monitoring and close-out of assigned study sites.
The CRA will be required to carry out the following duties at clinical investigation sites: Completeappropriate training sessions with ProjectLeads Identify and assess the suitability of facilities to be used as the device study/investigation site Conduct site monitoring in accordance with the study protocol/risk-ba...