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

Introduce yourself briefly

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Are you a Saudi national? (Please note: Only Saudi nationals will be considered for this position due to local employment regulations)

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Availability to start

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Availability to start

Immediately available

Available within 1 month

Available within 2 months

3+ months

Currently employed (notice period required)

Education

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Field of study (Examples: "Pharmacy", "Nursing", "Medicine", "Biology", "Public Health", "Clinical Sciences"...)

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University/Institution name

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Do you have a valid GCP (Good Clinical Practice) certification?

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Years of clinical research experience

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Please describe your clinical research experience (Check all that apply)

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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

If other, please specify below

Have you used Electronic Data Capture (EDC) systems?

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Which EDC system(s) have you used?

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Which EDC system(s) have you used?

Medidata Rave

Oracle InForm

REDCap

OpenClinica

Castor EDC

Other (please specify below)

None

If other, please specify below

Have you conducted Source Data Verification (SDV)?

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Computer proficiency

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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)

Have you performed monitoring visits at clinical trial sites?

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Types of clinical studies you've worked on

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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

Are you comfortable traveling for monitoring visits ?

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Are you comfortable with a remote/hybrid work model?

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Expected monthly salary in SAR

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Upload your CV in PDF format

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Size limit: 10 MB

Upload your GCP Certificate in PDF

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Size limit: 10 MB

Why are you interested in this CRA position with MFG?

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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)

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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)