TMF Specialist

TMF Specialist is to perform all duties related to the timely processing of essential and non-essential clinical trial documents to facilitate study startup, drug shipment, eTMF maintenance and support eTMF inspection readiness activities.

Preferred: 2 Years’ experience in Pharmaceutical or Contract Research Organization

Ability to interact with Clinical and Regulatory team regarding the receipt, analysis, classification and disposition of documents

Preferred: knowledge of “Essential Documents” Clinical Trial Documentation