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Hiring for Hiring for Clinical Document Management Chennai, Pune for Exp. 1 - 6 Years at Syntel Priv (Chennai Job)

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Job Description:Desired Skills and Competencies Any Life Science graduate with minimum 3 months experience in Clinical document management /Clinical data management/Clinical research Coordination Exposure to Medical coding / QA QC in clinical research / Regulatory affairs/ Regulatory publishing / PV is needed Should have knowledge of ICH GCP principles and Clinical drug development process Experience working on eTMF (Electronic Trial Master File ) tool is preferred Must be comfortable working in rotational shifts Interns in clinical research and clinical data management with 3 months of exposure too can apply Job Specification : The position requires dealing with clinical research documents, scrutiny, review and archiving Global responsibility for Trial Master File (TMF) quality for sponsor and/or CRO studies. Map the attributes as per migration requirement based on the content Ensure 100% quality adherence Maintain daily production and quality reports Communicate Daily queries to Client. Pro-actively highlight potential risks to the process in terms of timelines, TAT, Quality etc Contact Person -Shalakha or Mohini E-Mail - [email protected] [email protected] Contact Numbers -9923605849/7875753085

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Posted on: Thursday, 13 April, 2017  08:43
Expires On: Tuesday, 24 December, 2019  18:30

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