Job description

The Clinical Project Lead at IROS, part of the G42 Laboratory in Riyadh, is responsible for managing the full lifecycle of clinical trials, ensuring on-time, high-quality delivery of study activities. This role serves as the primary liaison between sponsors, study sites, and internal stakeholders and is tasked with overseeing all aspects of clinical trial execution. This includes managing EC/RA regulatory submissions, monitoring study milestones, tracking progress, and reporting updates. The Clinical Project Lead will conduct co-monitoring visits with Clinical Research Associates (CRAs), support their performance, and ensure monitoring report quality. The role also involves coordination with internal and external stakeholders and third-party vendors, development and approval of essential trial documents, oversight of investigator meetings, contract and logistics management, and supervision of team members. Adherence to ICH-GCP and internal SOPs is required. The candidate must have advanced knowledge of clinical trial phases I–IV, FDA regulations, and CTA processes, along with strong leadership, communication, and organizational abilities. The position is based in Riyadh and requires proficiency in English and Microsoft Office, with a valid driver’s license. Experience in a CRO or sponsor environment is preferred.