Senior CRA I

5 days ago

Toronto, Canada PSI CRO Full time

Job DescriptionAs a Senior CRA you will work on the frontline of communication with project stakeholders, ensuring timelines, targets and standards of clinical research projects in a variety of therapeutic indications.  You will build and maintain relationships with clinical sites and investigators.  You will focus on subjects’ rights, safety and well-being and quality of data compliance.Home-basedYou will:Conduct and report all types of onsite monitoring visitsBe involved in study startupPerform CRF review, source document verification and query resolutionBe responsible for site communication and managementSupervise study activities, timelines, and schedules on the country levelBe a point of contact for in-house support services and vendorsBe involved in quality control, such as compliance monitoring and reports reviewParticipate in feasibility researchSupport regulatory team in preparing documents for study submissionsQualificationsCollege/University degree in Life Sciences or an equivalent combination of education, training & experienceIndependent on-site monitoring experienceExperience in all types of monitoring visits in Phase II and/or IIIParticipation in clinical projects as a Lead/Senior MonitorExperience in OncologyFull working proficiency in English and FrenchProficiency in MS Office applicationsAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travelValid driver’s license (if applicable)Additional InformationMake the right call and take your career to a whole new level.  Join the company that focuses on its people and invests in their professional development and success.

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