Clinical Study Administrator - Conshohocken

Only for registered members Conshohocken, United States

1 month ago

Default job background
Full time

Job summary

The Clinical Study Administrator will be responsible for collecting and tracking documents for clinical trials. This includes assisting in timely submission of proper application/documents to EC/IRB and Regulatory Authorities.

Responsibilities include interacting with Investigators and CRAs during document collection process,
operational responsibility for local eTMF set-up and maintenance,
ensuring essential documents are uploaded on time,
supporting CRA in close out activities,
and contributing to production and maintenance of study documents.
  • Clinical trial support experience required.
  • Bachelor's degree with relevant experience.

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