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CRA (Level II)

M-264680 Pharmaceutical Product Development Spain SL·Remote

Pay not statedMid levelFull-timeRemote
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About the role

Ensures that required essential documents are complete and in place, according to ICH-GCP and applicable regulations. Conducts on-site file reviews as per project specifications. Facilitates effective communication between investigative sites, the client company and the PPD project team through written, oral and/or electronic contacts.

What you need

  • Clinical research
  • Communication
  • Any graduate

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