IQVIA

Clinical Research Associate, French-speaking

IQVIA

full-time

Posted on:

Location Type: Office

Location: Montreal • 🇨🇦 Canada

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Job Level

JuniorMid-Level

About the role

  • Participates in the preparation and conduct of Phase I–IV clinical trials.
  • Supervises the progress of clinical investigations by performing site assessment, initiation, and interim close-out visits.
  • Ensures monitoring of clinical trials in accordance with Good Clinical Practice (GCP) and procedures established by IQVIA.
  • Collaborates with the ISS team to coordinate site activities in preparation for study start.
  • Obtains regulatory documentation to enable successful implementation, monitoring, and assessment of clinical trials.
  • Performs source document verification according to sponsor requirements.
  • Reviews the quality and integrity of clinical data through internal review of eCRF data and on-site source verification.
  • Conducts study closeout visits in accordance with the study-specific clinical monitoring plan.

Requirements

  • BS/BA/BSc (or equivalent) in a life sciences or healthcare discipline (e.g., pharmacist, nurse, etc.) and a minimum of four (4) years' experience in site monitoring/site management required; or an equivalent combination of education, training, and experience.
  • At least four years' experience in oncology and/or medical devices.
  • Experience in monitoring and/or coordinating clinical trials required.
  • Valid driver's license.
  • Computer skills, including proficiency in Microsoft Word, Excel, and PowerPoint, and comfortable using a laptop.
  • Functional knowledge of English, both written and spoken, is required to perform this role.
Benefits
  • Reasonable accommodations for candidates with disabilities available upon request during the recruitment process.

Applicant Tracking System Keywords

Tip: use these terms in your resume and cover letter to boost ATS matches.

Hard skills
clinical trialssite monitoringsource document verificationclinical data reviewGood Clinical Practice (GCP)eCRF datastudy closeoutregulatory documentationoncologymedical devices