Submission Specialist - Raanana

Only for registered members Raanana, Israel

1 month ago

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Job Summary

You will facilitate the start of research projects of novel medicinal products while taking a step further in your professional career.


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Responsibilities

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  • Prepare clinical trial submission dossiers for Regulatory and Ethics Authorities.
  • Communicate with regulatory authorities, ethics committees, project teams and vendors on regulatory-related matters.
  • Review translations of essential documents subject to clinical trial submission.

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