Clinical Research Associate – Senior, Bilingual French/English

Parexel

. Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites .

Posted 10/2/2026full-timeRemote • CanadaSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical site management, ensuring compliance with protocols and regulatory requirements while maintaining strong site relationships. Proficient in patient recruitment strategies and data quality evaluation to support successful clinical trials.

Highest-signal resume keywords

Clinical Research Associate ExperienceSite MonitoringRegulatory ComplianceClinical Trial Management SystemsFluency in English and French

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Onsite MonitoringData Quality EvaluationPatient Recruitment StrategiesSite Document VerificationStudy Protocol Understanding

Soft Skills

Interpersonal CommunicationClient-Focused ApproachAbility to Work IndependentlyFlexibilityTime Management

Tools & Technologies

Clinical Trial Management SystemsElectronic Document Management SystemsMicrosoft ExcelMicrosoft Word

Industry Keywords

Good Clinical PracticeSOP ComplianceHuman-Subject RightsClinical TrialsBiological Science

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Conduct qualification visits, site initiation visits, monitoring visits, and termination visits at assigned clinical sites
Generate visit and contact reports
Build and maintain site relationships as the primary site contact
Address and resolve site issues and questions
Oversee study integrity and site delivery from identification through close-out
Review trial performance and safeguard human-subject rights and well-being in accordance with the protocol
Develop patient recruitment strategies with clinical sites to meet enrollment timelines
Ensure compliance with SOPs, protocols and amendments, GCP, and applicable regulatory requirements
Evaluate reported-data quality and integrity, site efficacy, and drug accountability
Monitor completeness and quality of regulatory documentation
Perform site document verification

Requirements

What you’ll need

18+ months of direct onsite monitoring experience as a Clinical Research Associate (CRA)
Bachelor's or equivalent degree in biological science, pharmacy, or another health-related discipline
Strong interpersonal, written, and verbal communication skills within a matrixed team
Ability to work independently with a sense of urgency and limited oversight
Client-focused approach and flexibility regarding assignments and new learning
Ability to manage multiple tasks, evaluate unpredictable scenarios, achieve project timelines, and apply understanding of study protocols
Honest and ethical work approach
Strong computer skills, including Clinical Trial Management Systems (CTMS), Electronic Document Management Systems (EDMS), Microsoft Excel, and Microsoft Word
Fluency in written and spoken English and French

Benefits

Comp & perks

Bonus incentive program
Less travel and a lower protocol load compared to industry peers
World-class technology
Training catered to individual experience
Opportunity to work within multiple therapeutic areas
Career advancement opportunities
Career growth support through consistent performance discussions and evaluations