scientific databases and search tools.

Critically analyze and summarize clinical data from published literature and other scientific sources.

Develop literature search protocols, screening strategies, and documentation.

Maintain strong working knowledge of global medical device approval pathways, with emphasis on EU MDR and European regulatory frameworks.

Demonstrate thorough understanding of Good Clinical Practice (GCP), applicable standards, and industry practices.

Maintain professional expertise by regularly reviewing clinical literature and contributing in cross-functional project meetings.

Understanding of Clinical Study related documents.

What you need:

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