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Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Independently manage all aspects of monitoring for assigned clinical trials across study phases, including site initiation, routine monitoring, and close-out visits.
- Ensure compliance with protocols, GCP, ICH, SOPs, and applicable regulatory requirements.
- Build strong site relationships, acting as a primary point of contact and ensuring high-quality data collection.
- Identify and resolve site issues, escalating as needed to maintain trial integrity and patient safety.
- Mentor and support junior CRAs, sharing knowledge and best practices.
Requirements
What you’ll need- Experience leading monitoring activities in complex trials, ideally in oncology or rare disease with a minimum of at least **2 years’ experience as independent site monitor**
- Strong understanding of **ICH-GCP** and **regulatory guidelines**
- Clear and confident communicator in **English and French**
- Comfortable working independently and managing priorities.
- Willingness to travel in France, as required.
Benefits
Comp & perks- Competitive salaries and a comprehensive benefits package
- Departmental Study/Training for furthering professional development
- Mentoring opportunities
- Internal growth opportunities and career progression
- Financially rewarding internal employee referral program
- Eligibility for our internal employee recognition programs for going above and beyond on projects
- Eligibility for our Loyalty Award Program in recognition of loyalty and commitment of longstanding employees
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
monitoring activitiesclinical trialsdata collectionsite initiationroutine monitoringclose-out visitsregulatory complianceGCPICHSOPs
Soft Skills
communicationrelationship buildingproblem solvingmentoringindependencepriority managementteam supportescalationconflict resolutionconfidence
