Senior Cra- Montreal / Quebec

As a Senior CRA you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.What you will be doing : The Sr. Clinical Research Associate will monitor the progress of clinical studies at investigative sites or remotely, and ensure clinical trials are conducted, recorded, and reported in accordance with the protocol, standard operating procedures (SOPs), ICH-GCP, and all applicable regulatory requirements.Applies knowledge of ICON’s policies and proceduresDemonstrates excellent written and oral communicationDemonstrates excellent knowledge of ICH / GCPDisplays ability to manage investigative sites to facilitate trial deliverablesDemonstrates ability to escalate issues appropriatelyConducts monitoring to confirm subject safety and data integrityDescribes and demonstrates the principals of IP accountabilityIdentifies scientific misconduct at the site levelDemonstrates working knowledge of Microsoft Office applications, Clinical Trial Management Systems, IVRS / IWRS and Electronic Data Capture platformsMentors CRAs new to the position or companyServes as an observation visit leaderConducts monitoring evaluation visitsAssists team lead in the development of trial tools or documentsAssists with CTM tasksParticipates in the development of process changes / improvementsPresents at client meetings / Investigator meetingsProvides training to trial teamsYou are : Undergraduate degree or its international equivalent in clinical, science, or health-related field from an accredited institution; a licensed health-care professional (i.E., registered nurse); or equivalent work experience requiredRead, write and speak fluent English; fluent in host country language required.2 years of experience supporting clinical trials including 1 year of on-site monitoring experience (for CRA2); 4 years of experience supporting clinical trials including 3 years of on-site monitoring experience (for CRA3)Ability to travel for approximately 10 site visits each monthProven success monitoring fast paced trials with quick turnaround times for database lockHigh proficiency with Microsoft Office and company collaboration applicationsAdvanced skill in utilization of applicable clinical systemsExperience in monitoring all trial components (PSSV to COV) is preferred