[Alexion] Clinical Research Associate

The Clinical Research Associate (CRA) has local responsibility for the delivery of the studies at their assigned sites and is an active participant in the local study team(s). The CRA works in close collaboration with local team members to ensure that study commitments are achieved in a timely and efficient manner on a site level.

Requirements

• Performing identification, selection, initiation, monitoring, site data review and closeout activities/visits
• Training, supporting, and advising Investigators and site staff in study-related matters
• Development of recruitment plans with each site and managing and supporting enrollment to ensure sites and studies meet enrollment milestones
• Ensuring timely collection/uploading of essential documents into the eTMF in accordance with ICH-GCP, Alexion SOPs and local requirements
• Preparing and finalizing monitoring visit reports in CTMS and provide timely feed-back to the Principal Investigator