About the jobTMF 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 activitiesLocation : Bangalore/ChennaiExperience Skills Ability to interact with Clinical and Regulatory team regarding the receipt, analysis, classification and disposition of documentsPreferred: 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 skillsProficient in use of MS office software including Word, Excel, Access, Share Point OutlookBachelors degree in Sciences requiredPreferred: 2 Years experience in Pharmaceutical or Contract Research Organization.Please use the below link for job application and quicker response.https://lifelancer.com/jobs/view/8226e40e7b6847a67d9da4694532acae