Turn this role into an interview — a resume and cover letter built around what this employer wants.
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
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Availability to start
Immediately available
Available within 1 month
Available within 2 months
3+ months
Currently employed (notice period required)
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Please describe your clinical research experience (Check all that apply)
Clinical Research Coordinator (CRC) in hospital/research center
Site coordinator for clinical trials
Hospital pharmacy with clinical trial exposure
Clinical data management
Regulatory affairs
Other (please specify below
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Which EDC system(s) have you used?
Medidata Rave
Oracle InForm
REDCap
OpenClinica
Castor EDC
Other (please specify below)
None
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Computer proficiency
Microsoft Excel (intermediate to advanced)
Microsoft Word (professional reports)
Video conferencing tools (Zoom, Teams)
Cloud-based collaboration tools (Google Drive, SharePoint)
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Types of clinical studies you've worked on
Phase I
Phase II
Phase III
Phase IV
Real-world evidence studies
Not applicable
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Size limit: 10 MB
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Size limit: 10 MB
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I agree that my personal data submitted in this form may be processed by Monitoring Force Gulf for recruitment purposes, in accordance with Saudi Arabia's Personal Data Protection Law (PDPL)