Parexel
Parexel
Parexel is a global clinical research organization serving biopharmaceutical companies throughout the development of new medicines. Its work spans Phase I–IV clinical trials, portfolio and trial management, regulatory strategy, market access, and lifecycle planning. With more than 21,000 professionals, Parexel combines clinical, regulatory, and therapeutic expertise with patient insights and innovative trial designs. The company supports research across areas including oncology, neuroscience, and rare diseases, with a focus on making clinical development more efficient and patient-centered.

Senior Bilingual Clinical Research Associate (French/English) – Canada Remote

Parexel is hiring a senior bilingual Clinical Research Associate to monitor clinical trials across Canada. The role manages site relationships, compliance, data quality, and study execution from site identification through close-out.

Description

  • Conduct site qualification, initiation, monitoring, and termination visits at assigned clinical sites
  • Prepare visit and contact reports
  • Serve as the primary contact for building and maintaining clinical site relationships
  • Investigate and resolve site questions and operational issues
  • Protect study integrity and oversee site delivery from identification through close-out
  • Assess trial performance and protect human-subject rights and well-being in line with study protocols
  • Partner with clinical sites to create patient recruitment strategies that support enrollment timelines
  • Maintain compliance with SOPs, protocols and amendments, GCP, and applicable regulatory requirements
  • Assess reported-data quality and integrity, site performance, and investigational drug accountability
  • Track the completeness and quality of regulatory documentation
  • Verify site documentation

Requirements

  • At least 18 months of direct on-site monitoring experience as a Clinical Research Associate (CRA)
  • Bachelor’s degree or equivalent in biological science, pharmacy, or another health-related field
  • Strong interpersonal, written, and verbal communication skills for working within a matrixed team
  • Ability to work independently, act with urgency, and operate with limited supervision
  • Client-oriented mindset with flexibility toward assignments and continued learning
  • Ability to prioritize multiple tasks, assess changing situations, meet project timelines, and apply study-protocol knowledge
  • Consistently honest and ethical approach to work
  • Strong computer proficiency, including Clinical Trial Management Systems (CTMS), Electronic Document Management Systems (EDMS), Microsoft Excel, and Microsoft Word
  • Fluent written and spoken English and French

Benefits

  • Eligibility for a bonus incentive program
  • Reduced travel and protocol workload compared with industry peers
  • Access to advanced workplace technology
  • Training tailored to individual experience
  • Exposure to multiple therapeutic areas
  • Opportunities for career advancement
  • Ongoing career development through regular performance discussions and evaluations

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