Job Description
Role and Responsibilities:
? Initiate start up meetings with the Study Teams related to the creation and development of the clinical document for regulatory submission.
? To work in coordination with all the members in the study team- internal and external for the development of clinical documents.
? Project timelines amongst the study team for the development of document.
? Prepare Clinical Documents according to the Standard Operating Procedures, Document Standards and ...
Shine.com - 30+ days ago
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