Associate, Study Management III/CTM III

📋 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