Junior Clinical Research Associate

We're a Franco‑Saudi CRO helping international pharmaceutical companies conduct clinical trials across the GCC. We need a field‑ready clinical research professional who can:✓ Monitor clinical trial sites independently with remote guidance✓ Conduct rigorous Source Data Verification (SDV) and ensure GCP compliance✓ Collaborate seamlessly with our Paris CRA team and UAE hospital sites✓ Manage site relationships professionally with minimal supervision.

• Monitor clinical trial sites independently with remote guidance.
• Conduct rigorous Source Data Verification (SDV) and ensure GCP compliance.
• Collaborate seamlessly with our Paris CRA team and UAE hospital sites.
• Manage site relationships professionally with minimal supervision.

• Valid GCP (Good Clinical Practice) certification.
• Minimum of 2 years of clinical research experience.
• Proficient in electronic data capture systems such as Medidata Rave, Oracle InForm, REDCap, Open Clinica, Castor EDC.
• Strong computer proficiency – Microsoft Excel (intermediate to advanced), Microsoft Word, Zoom/Teams, Google Drive/SharePoint.
• Experience monitoring visits at clinical trial sites and familiarity with Phase I–IV studies.

Only Saudi nationals will be considered for this position due to local employment regulations.

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