Medical Writer

1 - 3 years

2 - 3 Lacs

Posted:1 day ago| Platform: Naukri logo

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Work Mode

Work from Office

Job Type

Full Time

Job Description

Role & responsibilities

  • To prepare protocol preparation
  • Incorporate the protocol comments received from Investigator, QC, QA, BR and Sponsor before finalization of the same.
  • To prepare informed Consent Documents (ICD) in English and coordinate for translation into Local language(s) and its back translation into English, if applicable.
  • To Prepare of the CRFs and other working documents, if applicable.
  • To prepare documents for submission to the regulatory.
  • Internal QC of study documents
  • Literature Search
  • To assist the Project Manager for feasibility assessment of study proposal.
  • Literature survey for PK & Safety study
  • Co-ordination with Principal Investigator (PI) and/or Clinical Investigator (CI) for application.
  • To prepare documents for submission to the Ethics Committee (EC).

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