Global Trial Acceleration Associate

About the role

This individual contributor role has task-level responsibility for clinical trial related document collection, compilation, review and approval across all phases of global clinical trials. This may also include review of all the Site Monitoring Visit reports, issue escalation, resolution and follow up tasks.

What you'll do

• The Global Trial Acceleration Associate is responsible for managing and executing on centralized activities in support of global trials with an emphasis on clinical…
• The Global Trial Acceleration Associate will interact with clinical study sites, CROs/vendors, Country Trial Managers (CTM)/Clinical Trial Monitor (CTMo.)
• As the main point of contact for essential document management, ethical and regulatory submission-related activities
• Support outsourcing activities by interfacing with operational teams, support groups and service providers for successful selection
• Initiate and manage start-up documentation activities for global clinical trials

What you need

• Clinical research
• Documentation
• Quality control
• Communication