Job Summary

• The role serves as an expert ensuring delivery of a centrally managed study management service across clinical studies from start up to reporting.
• The incumbent acts as the main contact for the Document Management group until the Clinical Study Report is finalised.
• The position requires maintaining deep knowledge of best practices and internal regulations while acting as a technical owner within Patient Safety.

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Skills & Requirements

Key Requirements

• Bachelor's degree in relevant discipline
• Experience of Study Management within a pharmaceutical or clinical background
• Knowledge of relevant legislation and new developments in the area of Clinical Development

Work Rights