ensuring compliance with regulatory standards, and driving continuous improvement initiatives. This position is a permanent, full-time position (40-hours per week) that will be based at Baylis Medical Technologies Inc.’s office at 26[...]

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[...]

Job summary: Under the VP Operations’ supervision, the Planning Coordinator is responsible for sequencing the lots to produce, to verify availability of components and raw materials. Responsibilities Sequence manufacturing and packag[...]

Working within Regulatory Affairs, reporting to Head, Regulatory Affairs, Associate, Quality & Regulatory Affairs is responsible for performing the required tasks related to Regulatory Affairs.  Principal Responsibilities Regulatory A[...]

or other software, to develop custom programming code to generate summary tables, data listings, graphs and derived datasets as specified in the statistical analysis plan and programming specifications. Works to ensure that outputs mee[...]

Description Results Analysis Scientist I Syneos Health® is a leading fully integrated biopharmaceutical solutions organization built to accelerate customer success. We translate unique clinical, medical affairs and commercial insights[...]

responsible for managing early-phase clinical studies (Phase I and Phase II) on a global scale. Ideal candidates should have extensive experience leading global clinical trials, particularly in early-phase studies, with a focus on oper[...]

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 [...]