Clinical research Jobs

Clinical Research Associate (based in Montreal) Position open to Canadian citizen\resident or with Canadian work permit Montreal Health Innovations Coordinator Center Full Time The Montreal Health Innovations Coordinating Center (MHICC[...]

Project Manager (Clinical Studies Phase II to IV) Position open only to Canadian citizen\resident or with Canadian work permit Montreal Health Innovations Coordinator Center Full Time The Montreal Health Innovations Coordinating Center[...]

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[...]

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 [...]

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[...]

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[...]

site initiation, interim monitoring, site management activities and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. Uses judgment an[...]