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Starhold in Saudi Arabia seeks a field-ready clinical research professional to monitor trial sites remotely, perform SDV, and ensure GCP compliance. You will collaborate with the Paris CRA team and UAE hospital sites while professionally managing site relationships with minimal supervision.
This role may involve travel within the GCC and occasional remote work. A strong background in clinical research operations is preferred.
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)