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 * * * * * Are you a Saudi national? (Please note: Only Saudi nationals will be considered for this position due to local employment regulations) * Availability to start * Availability to start Immediately available Available within 1 month Available within 2 months 3+ months Currently employed (notice period required) Education * Field of study (Examples: "Pharmacy", "Nursing", "Medicine", "Biology", "Public Health", "Clinical Sciences"...) * University/Institution name * Do you have a valid GCP (Good Clinical Practice) certification? * Years of clinical research experience * Please describe your clinical research experience (Check all that apply) * 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? * Which EDC system(s) have you used? * Which EDC system(s) have you used? Medidata Rave Oracle In Form REDCap Open Clinica Castor EDC Other (please specify below) None If other, please specify below Have you conducted Source Data Verification (SDV)? * Computer proficiency * Computer proficiency Microsoft Excel (intermediate to advanced) Microsoft Word (professional reports) Video conferencing tools (Zoom, Teams) Cloud-based collaboration tools (Google Drive, Share Point) Have you performed monitoring visits at clinical trial sites? * Types of clinical studies you've worked on * 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 ? * Are you comfortable with a remote/hybrid work model? * * Expected monthly salary in SAR * Upload your CV in PDF format * Size limit: 10 MB Upload your GCP Certificate in PDF * Size limit: 10 MB Why are you interested in this CRA position with MFG? * 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) * 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) #J-18808-Ljbffr