Study-level oversight and leadership of one or more global trials in a cross-functional environment
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
Co-development and management of study materials, including protocols, regulatory submissions, and

🎯 Requirements

Bachelor’s Degree or OUS equivalent required
At least 4 years of progressive Pharma-related/clinical research-related experience
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

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