About the job
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
Location : Bangalore/Chennai
Experience Skills
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
Bachelors degree in Sciences required
Preferred: 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
India
