Study Project Manager I - Oncology

Role: Clinical Study Project Manager I responsible for planning, executing, and overseeing clinical research studies across all development stages, ensuring quality, efficiency, and regulatory compliance. Responsibilities include defining operational strategies, managing budgets/timelines, vendor oversight, risk mitigation, and leading cross-functional study teams from initiation through to completion. Requirements: Bachelor's degree, 6+ years of pharma or clinical research experience, ideally with exposure to Phase 1-4 or medical device trials. Preferred skills include clinical study operations management, vendor negotiation, and stakeholder engagement. High-Value: Focus on clinical operations in pharmaceutical development, with experience in study design, budget management, vendor oversight, and cross-functional team leadership. Emphasis on GxP compliance and global study execution. WorkSetup: Not specified; the role may involve collaboration across global teams.