Associate, Study Management III/CTM III

About this role

📋 Description Study-level oversight and leadership of one or more global trials in a cross-functional environment Supports the Study Project Manager in strategic leadership of the cross-functional team through Vendor management, including RFP/initiation, selection, Scope of Work development & review Recruitment management, including review of intelligence data, leadership, cross-functional Leadership of assigned meetings and provision of regular updates on study status Risk identification, mitigation, and management, including timely issue review, escalation, and 🎯 Requirements Bachelor’s Degree or OUS equivalent required At least 4 years of progressive Pharma-related/clinical research-related experience with a high Competent in application of standard quality procedures (SOP, ICH/GCP, Global Regulations) Experienced user of systems such as EDC, IRT, CTMS, and eTMF Strong analytical and critical thinking skills Excellent organizational and time management skills, strong attention to detail

Source listing: empllo_remote