- 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
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TMF Specialist
Found in: Talent IN 2A C2 - 1 day ago
ICON Strategic Solutions Chennai, IndiaTMF 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 Phar ...
TMF Specialist - Chennai, India - ICON Strategic Solutions
Description
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.