
Clinical Research Associate, French-speaking
IQVIA
full-time
Posted on:
Location Type: Office
Location: Montreal • 🇨🇦 Canada
Visit company websiteJob 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