as necessary. Represents the Medical Writing department on clinical study teams, at conferences, meetings and for presentations to the client regarding a writing project. Advises clients and study teams on data presentation and product[...]
Standard Operating Procedures and Work Instructions Assists Clinical Monitoring staff with site management activities, including serving as a Sponsor representative for sites on assigned studies, and communicating with sites to ensure [...]
site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practices (GPP) and protocol compliance. Uses judgment and experien[...]
site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment and experienc[...]
as necessary. Acts as lead for assigned writing projects. Manages medical writing activities associated with individual studies, coordinating medical writing activities within and across departments with minimal supervision. Develops o[...]
Acts as a site processes specialist, ensuring that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations and SOPs to guarantee subjects rights, well-being and data reliability. Ensu[...]
Current Employees apply HERECurrent Contingent Workers apply HERESecondary Language(s) Job Description:Chef des associé(e)s, Recherche clinique Localisation: Greater Toronto Area (GTA), OntarioCe rôle sera essentiel pour faire un sui[...]