Senior CRA

Company DescriptionWe are the company that cares – for our staff, for our clients, for our partners and for the quality of the work we do. A dynamic, global, mid-size company founded in 1995, we bring together more than 3,000 driven, dedicated and passionate individuals. We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.Job DescriptionWe are looking for an experienced freelance Sr. CRA to support us with the following responsibilities in Canada:Conduct and report SIV, RMV, COV onsite monitoring visitsPerform CRF review, source document verification and query resolutionBe responsible for site communication and managementBe a point of contact for in-house support services and vendorsCommunicate with internal project teams regarding study progressParticipate in feasibility researchSupport regulatory team in preparing documents for study submissionsPrepare and particiapte on audits and inspectionsQualificationsCollege/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 IIIExperience in Oncology is a plusFull working proficiency in English and French is essential.Proficiency in MS Office applicationsAbility to plan, multitask and work in a dynamic team environmentCommunication, collaboration, and problem-solving skillsAbility to travelValid driver’s licenseAdditional InformationThis is a great opportunity for you to further develop your skills, widen your therapeutic area experience, and become an expert in clinical research. Compensation: CAD 120000 - CAD 150000 - yearly

The Senior CRA is responsible for conducting onsite monitoring visits, including SIV, RMV, and COV, while managing site communications and CRF reviews. They also support regulatory submissions, participate in feasibility research, and prepare for audits and inspections.

Candidates must hold a degree in Life Sciences and have independent on-site monitoring experience in Phase II and/or III trials. Full working proficiency in both English and French, along with a valid driver's license, is essential.

Relevées dans la description du poste. Confirmez les exigences importantes ci-dessus.

• On-site Monitoring
• CRF Review
• Source Document Verification
• Site Management
• Feasibility Research
• Regulatory Documentation
• Audit Preparation
• Oncology
• English Proficiency
• French Proficiency
• MS Office
• Multitasking
• Problem-solving
• Collaboration
• Clinical Research
• Project Communication

• Healthcare
• Science & Research

Formation minimale

Baccalauréat

Expérience minimale

5+ ans

Langue de l’offre

anglais

Heures de travail

40 heures par semaine