Bilingual French Clinical Research Associate monitoring clinical trials for pharmaceutical and biotech sponsors. Ensuring site compliance, data integrity and audit readiness across remote and on - site visits.
About the role
- Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organization. Ensuring protocol, ICH-GCP, and regulatory compliance across investigative sites and remote studies.
Responsibilities
- Monitor the progress of clinical studies at investigative sites or remotely
- Ensure clinical trials are conducted, recorded, and reported according to the protocol, SOPs, ICH-GCP, and applicable regulatory requirements
- Support clinical research for pharmaceutical, biotechnology, medical device, government, and public health organizations
- Travel up to 70%
Requirements
- Bachelor's degree, or its international equivalent in a scientific or health-related field, or an equivalent combination of education and clinical research experience
- 1+ years of clinical monitoring experience or equivalent combination of education and experience for the level 2 role
- 3+ years of clinical monitoring experience for a level 3 role
- Oncology monitoring experience preferred
- Ability to travel 70%
- Knowledge of ICH and local regulatory authority regulations regarding drug trials
- Legally authorized to work in the United States or Canada
- Must not require, now or in the future, sponsorship for employment visa status
- Bilingual English/French required
Benefits
- Competitive base salary and performance related incentives
- Health and wellbeing programmes including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life assurance and disability coverage
- Employee assistance programmes and wellbeing resources
- Learning and development opportunities through structured training and career pathways
- Supportive policies and wellbeing initiatives
- Reasonable accommodations during the recruitment process
Job title
Job type
Experience level
Salary
Degree requirement
Tech skills
Location requirements
Report this job
Found something wrong with the page? Please let us know by submitting a report below.
Clinical Research Associate II conducting onsite monitoring and regulatory support for PSI, a contract research organization. Managing sites, CRF review, queries, and study progress across clinical trials.
Senior Clinical Research Associate conducting onsite monitoring and regulatory activities for a global medical research company. Supporting Phase II/III studies and Canadian clinical - trial sites.
Clinical Research Associate monitoring investigative sites and clinical trials for AbbVie’s innovative medicines pipeline. Ensuring patient safety, data integrity, compliance, and recruitment performance.
Clinical Research Associate monitoring Novo Nordisk clinical trials across Greater Montreal. Ensuring site compliance, patient safety, data integrity and timely study delivery.
Senior Clinical Scientist leading oncology clinical trials for ICON’s sponsor - dedicated research programs. Providing medical monitoring, scientific oversight, and protocol execution across US and Canadian locations.
Clinical Research Associate monitoring clinical trials for ICON, a global healthcare intelligence and clinical research organization. Ensuring protocol, ICH - GCP, and regulatory compliance across investigative sites.
Clinical Scientist interpreting WES/WGS data and classifying variants for SeqOne, a clinical genomics company. Supporting rare - disease diagnostics through regulated, patient - centered genomic reporting.
Clinical Research Associate monitoring clinical trial sites for Parexel, a global clinical research organization. Ensuring patient safety, data quality, regulatory compliance, and site delivery.
Clinical Research Associate monitoring clinical trials for ICON’s global healthcare research organization. Ensuring protocol, ICH - GCP, SOP, and regulatory compliance across investigative sites and remote work.