Description

You will support global clinical studies by collaborating with cross-functional teams and overseeing CROs and vendors to ensure studies are conducted on time and within budget. You'll assist with study start-up, document management, tracking study progress, and maintaining compliance with regulatory standards.

Requirements

• BS in life sciences
• 3-5 years of biotech/pharmaceutical clinical operations experience

Responsibilities

• Collaborate with cross-functional teams to coordinate clinical studies
• Oversee CROs and vendors, ensuring adherence to scope and timelines
• Assist with study start-up activities including document development
• Review and track CRO monitoring visit reports and resolve issues
• Maintain trial master files and internal trackers