Study Project Manager I - Oncology

📋 Description

• Define and drive operational strategies and deliverables for clinical studies
• Execute clinical studies in compliance with ICH/GCP and regulations
• Manage budget, timelines, and study issues proactively
• Lead cross-functional Clinical Study Teams in matrix environment
• Manage vendors and external stakeholders effectively
• Develop study design, systems, tools, and documents

🎯 Requirements

• Bachelor's degree or equivalent required
• 6+ years pharma/clinical research experience required
• Experience in Phase 1-4 study initiation to completion preferred
• Medical device trial experience preferred

🎁 Benefits

• Paid time off (vacation, holidays, sick)
• Medical, dental, and vision insurance
• 401(k) plan
• Long-term incentive programs