French-fluent Clinical Research Associate work in Quebec, monitoring Phase I-IV trials and device studies through onsite and remote visits.
Premier Research seeks a Clinical Research Associate II or Senior Clinical Research Associate with four-plus years of onsite monitoring experience. You will support oncology, pediatrics, rare disease, and other clinical studies while protecting data integrity and patient safety. The work includes investigative-site communication, trial documentation, and visit management.
Key Responsibilities:
- Conduct qualification, initiation, monitoring, management, and closeout visits
- Verify clinical data validity, correctness, completeness, and integrity
- Manage site queries and support Trial Master File activities
- Identify risks and investigative-site retraining opportunities
- Plan visits, trip reports, and study deliverables
Requirements:
- Undergraduate degree or international equivalent
- Four-plus years of onsite clinical research monitoring experience
- French fluency and residence in Quebec
- Ability to complete eight to ten monitoring visits monthly
- Valid driver's license and passport as required
Apply clinical monitoring, French fluency, and site-management expertise across patient-focused studies with Premier Research in Quebec.
Senior Clinical Research Associate Quebec in Ottawa employer: Premier Research Group
At Premier Research, we pride ourselves on being an exceptional employer that values innovation and collaboration in the healthcare sector. Our remote work culture fosters flexibility and inclusivity, allowing you to thrive while making a meaningful impact in dermatology. With ample opportunities for professional growth and a commitment to employee well-being, you'll find a rewarding career path that aligns with your passion for transforming patient care.
