Clinical Study Administrator - Conshohocken
1 month ago

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.
Job description
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