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

• 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

• Good verbal and written communication skills (English and local)

• Attention to detail and ability to multi-task

• Strong problem solving, time management, and organizational skills

• Proficient in use of MS office software including Word, Excel, Access, Share Point Outlook

• Bachelor’s degree in Sciences required

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