Associate, Study Management III/CTM III

📋 Description

• Study-level oversight and leadership of one or more global trials in a cross-functional environment
• Vendor management, including Request for Proposal (RFP)/initiation, selection, Scope of Work
• Recruitment management, including thoughtful review of intelligence data, leadership
• Leadership of assigned meetings (cross-functional (internal), vendor, and/or investigator) and
• Co-development and management (review, revision, tracking and filing) of study materials, including
• CTMS and eTMF management to ensure compliance/inspection readiness, support trend analyses and

🎯 Requirements

• Bachelor’s Degree or OUS equivalent
• Must have at least 4 years of progressive Pharma-related/clinical research-related experience with
• 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 to evaluate complex issues from multiple
• Excellent organizational and time management skills, strong attention to detail