Global Clinical Study Manager

Responsibilities

• Lead global cross-functional study team and ensure effective decision making
• Ensure alignment of study goals with corporate objectives and deliverables
• Manage planning and execution of clinical studies from feasibility to closeout
• Oversee quality and risk management, ensuring compliance with protocols and regulations
• Manage study budgets and vendor selection, ensuring effective resource utilization

Qualifications

• 6+ years of progressive experience in clinical research within biotech, pharma or CRO industries
• Proven project management experience in global clinical studies, preferably in oncology
• Advanced knowledge of clinical operations methodologies and study processes
• Bachelor's Degree in a scientific or healthcare discipline is required; higher degree preferred

Benefits

• Comprehensive benefits package including Medical, Dental, and Vision coverage
• 401(k) plan with company matching contributions
• Paid Time Off and Wellness programs
• Opportunities for equity ownership in the company through discretionary awards
• Flexible Spending Account/Health Savings Account options