Job Summary

• The role provides administrative and operational support to the Clinical Research Manager for preclinical and clinical studies across all phases.
• Primary responsibilities include organizing, maintaining, and performing quality checks on both paper and electronic Trial Master Files using Veeva and other repositories.
• The position involves coordinating clinical supplies, managing shipping logistics, and supporting regulatory submissions in compliance with internal SOPs.

Matching Summary

Skills & Requirements

Key Requirements

• Knowledge of clinical trial operations
• Experience with TMF management systems
• Ability to work with CROs and external vendors

Work Rights