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.ResponsibilitiesMonitor 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.QualificationsValid 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, OpenClinica, 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.EligibilityOnly Saudi nationals will be considered for this position due to local employment regulations.EEO StatementI 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