Clinical Trial Project Manager

‏⁦⁩Job PurposeOwns full end-to-end delivery of both clinical trail studies — scientific, regulatory, operational, and commercial coordination — acting as the single accountable point of contact internally a, the university partner, SFDA, the central laboratory, and the clinical site.Key Responsibilities● Hold overall responsibility for timeline, budget, and quality across both studies from protocol finalization through final study report.● Coordinate the ethics/IRB and SFDA submission process end-to-end, including query response management.● Manage all vendor relationships (central lab, EDC/ePRO platform, courier, site) and their contracts/SOWs.● Serve as the primary relationship owner with xxxl and the university, including all governance commitments (registration, SAP, data access, publication rights).● Chair regular internal and cross-stakeholder project status meetings; escalate risks and resolve issues proactively.● Oversee site initiation, monitoring cadence, and staff training in coordination with the CRA.● Own the risk register and change-control process for both studies.Requirements & Qualifications● Bachelor's degree in life sciences, pharmacy, or related field (Master's or clinical background preferred).● Minimum 5–7 years' experience in clinical trial project management within a CRO, pharmaceutical company, or contract research setting.● Demonstrated experience managing SFDA and/or IRB submissions in Saudi Arabia.● Strong vendor and budget management experience.● Excellent stakeholder management and written/verbal communication in English and Arabic.● GCP certification required.