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CRA Consultant, Junior Clinical Research Monitor
Ividata Life SciencesConsultant ARC monitoring clinical trials for IVIDATA Life Sciences with significant projects in health innovation. Requires expertise in Phases II/III and oncology experience.
About the role
Key responsibilities & impact- Ensure the setup, monitoring and close-out of investigational sites
- Conduct on-site monitoring (7 to 8 trips per month)
- Verify source data consistency (SDV) and compliance with GCP/ICH
- Manage study logistics
- Identify and resolve on-site issues
- Write visit reports and track corrective actions
- Maintain clear communication between the sponsor and investigational sites
Requirements
What you’ll need- Master's degree in a scientific field (MSc), PhD, or Pharmacist
- 1–3 years' experience monitoring interventional clinical research in a CRO or pharmaceutical company
- Experience with Phase II and III clinical trials
- Proficiency with EDC and CTMS systems
- Knowledge of French and European regulations
- Experience in oncology
- Professional proficiency in English (written and spoken) required
Benefits
Comp & perks- Stimulating work environment
- Involvement in health innovation
- High-impact assignments and a people-centered culture
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
monitoringsource data verificationGCPICHstudy logisticsvisit report writingcorrective action trackingclinical trial managementinterventional clinical researchoncology
Soft Skills
communicationproblem-solvingorganizational skills
Certifications
Master's degreePhDPharmacist