Perform all aspects of CRA duties from site selection, site initiation, through to site routine monitoring visits through to close-out visits (on-site and remote) and database lock
You will be fully embedded in our client's study team and have a dedicated ICON functional manager to support you
Oversees all aspects of study site management to ensure high quality data resulting in consistently low query levels and in good Quality Assurance reports
Qualifications
Degree in Pharmacy or any related course
2+ years prior monitoring experience with global trials within CRO or pharmaceutical company
Excellent written and verbal communication skills
Strong knowledge of international guidelines ICH-GCP, as wel as of local regulations
Flexibility to travel and to work from the sponsor occasionally during onboarding (if not traveling)
