... supplier and co-manufacturing sites to ensure safe, compliant, and ... supplier and co-manufacturing sites to ensure safe, compliant, and ... and co-manufacturing sites to ensure safe, compliant, and ... and co-manufacturing sites to ensure safe, compliant, and ...
... returned. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness ... Project Manager Proactively suggest potential sites based on local knowledge of ... 200 Studies across 73,000 Sites and 675,000+ Trial patients. ...
... returned. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness ... Project Manager Proactively suggest potential sites based on local knowledge of ... 200 Studies across 73,000 Sites and 675,000+ Trial patients. ...
... resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query ... requirements. • Provides guidance at the site and project level towards audit ... 200 Studies across 73,000 Sites and 675,000+ Trial patients. ...
... resolution techniques remotely and on site, and provides guidance to site staff as necessary, driving query ... requirements. • Provides guidance at the site and project level towards audit ... 200 Studies across 73,000 Sites and 675,000+ Trial patients. ...
... maintain good rapport with study sites;a.maintain frequent telephone communication with sites, providing guidance to study coordinators and investigators as necessary and ... English Ability to manage the sites independently Why ICON? Our focus ...
... returned. Routinely reviews the Investigator Site File (ISF) for accuracy, timeliness ... in the clinical team; manages site-level activities communication to ensure ... 200 Studies across 73,000 Sites and 675,000+ Trial patients. ...
... . Serves as primary contact for site personnel, acting as liaison between site personnel and sponsor study team ... of reported data, ensuring that sites enter data into EDC and ... 8-10 days month on site. Candidates must be located on ...
... , monitoring and closure of assigned sites in clinical studies, in compliance ... .g. protocol amendment submissions, Investigator site budget negotiation. If responsible for ... all trial components (pre-study site visit [PSSV] to closeout visit [ ...
... the oversight of Country and Site Trial Master Files (TMF). During ... local processes. • Identify problems at sites; resolve issues and escalate as ... • Review and manage data at site; resolve technical and content issues ...