Principal Global Trial Associate

Provides operational support for global insourced or outsourced, Non-Registrational Data Generating or Registrational Data Generating interventional clinical trials from concept to final clinical study report. May be responsible for a clinical trial(s) in the maintenance or close-out phases of its life cycle.

Requirements

• Project management concepts to support management of issues, risks, timelines, and budget
• Development and/or collection of study level documentation
• eTMF accuracy and completion for all studies
• Country planning, protocol level attributes, and milestones/drivers in CTMS

Benefits

• Competitive benefits, services, and programs
• Wide variety of benefits
• Resources to pursue goals, both at work and in personal lives