Global Study Associate

Trzdev28

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Experience with electronic trial master file
Knowledge of ich/gcp guidelines
Proven organizational and analytical skills
** The Global Study Associate position at Trzdev28 focuses on supporting Global Study Leaders and managing electronic trial documentation in compliance with industry standards. The ideal candidate will possess a background in medical or biological sciences, strong organizational skills, and proficiency in administrative tasks, contributing to the overall success of clinical research projects. **

Job Summary

  • The role involves supporting Global Study Leaders and managing clinical study documentation.
  • You will ensure compliance with regulatory guidelines and maintain study materials.
  • Collaboration with various stakeholders is essential for successful project execution.

Matching Summary

Match Score: 75

** The Global Study Associate position at Trzdev28 focuses on supporting Global Study Leaders and managing electronic trial documentation in compliance with industry standards. The ideal candidate will possess a background in medical or biological sciences, strong organizational skills, and proficiency in administrative tasks, contributing to the overall success of clinical research projects. **

Skills & Requirements

Must-have

  • Experience with electronic Trial Master File
  • Knowledge of ICH/GCP guidelines
  • Proven organizational and analytical skills

Nice-to-have

  • Excellent verbal and written communication
  • Ability to work independently and in teams
  • Willingness to train others

Key Requirements

  • Education in medical or biological sciences preferred
  • Previous administrative training or experience
  • Develop working knowledge of the Clinical Study Process

Work Rights

Not specified

Tailored Resume

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