Study Coordinator I

About the role

With our global scale and deep expertise, you’ll have the opportunity to do meaningful work, grow your career and make a real impact on people’s health around the world. Together, we’re improving health and improving lives.

What you'll do

• Coordinate study activities, including protocol preparation, study scheduling, milestone tracking, and status updates using study outlines and client-provided information
• Monitor study progress against agreed plans, identify potential delays or risks, and proactively follow up on critical milestones
• Coordinate study initiation activities, pre-initiation meetings, and other study-related discussions
• Support the coordination of multiple studies simultaneously, prioritizing activities based on timelines, complexity, and business needs
• Review study activities for consistency with approved protocols, applicable SOPs, client-specific requirements, and relevant regulatory guidelines

What you need

• 2–5 years in operations
• Coordination
• SOP writing
• Any graduate

Good to have

• Excel
• Reporting