Senior Data Coordinator - DM

About the role

You will help biotech, medtech, and specialty pharma companies transform life-changing ideas and breakthrough science into new medicines, devices, and diagnostics. What we do is profoundly connected to saving and improving lives, and we recognize our team members are the most valuable asset in delivering success.

What you'll do

• Prepare and maintain clinical data management documentation, including CRF Completion Guidelines (CCGs), Data Management Plans (DMPs), Data Report Specifications
• Support the development of standard test data for testing database screens and listings, provide feedback on test results, and perform User Acceptance Testing (UAT)
• Assist with clinical database set-up, maintenance, updates, and related data management activities
• Review CRFs, data listings, and clinical databases to ensure data accuracy, completeness, and consistency with study protocols, CCGs, DMPs, and applicable procedures
• Generate and manage data queries with appropriate internal and external stakeholders, including investigational sites, Clinical Research Associates (CRAs)

What you need

• 4–7 yrs of experience
• Clinical data management
• Clinical research
• Reporting
• Documentation
• Reconciliation
• Any graduate