The role involves assisting Clinical Research Associates and the Regulatory team in maintaining clinical documents and systems like the Trial Master File
Job Summary
The role involves assisting Clinical Research Associates and the Regulatory team in maintaining clinical documents and systems like the Trial Master File.
Candidates will help manage the preparation, distribution, and archiving of clinical documentation while ensuring compliance with standard operating procedures.
The position requires awareness of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines as part of company training.
Matching Summary
The role involves assisting Clinical Research Associates and the Regulatory team in maintaining clinical documents and systems like the Trial Master File.