Job Summary

• Join a global team supporting over 2,700 clinical trials across 100+ countries with top pharmaceutical and biotech companies.
• The role involves coordinating trial activities, supporting audit readiness, and providing administrative support for site activation and regulatory submissions.
• You will collaborate with internal departments and external sites to ensure high-quality, timely completion of trial tasks and maintain compliance with SOPs and regulatory guidelines.

Matching Summary

Skills & Requirements

Key Requirements

• High school diploma or equivalent
• Relevant clinical trials experience
• Knowledge of Country Regulations and SOPs
• Advanced English proficiency
• Bachelor's degree preferred

Work Rights