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Clinical Trial Assistant @ INC Research | Life Sciences Candidates Apply Online

This job expires in :

-317Days -17Hours -51Minutes -54Seconds


Join an industry-changing company that is reinventing the way we develop and commercialize drugs. At INC Research/inVentiv Health our 22,000 employees have one purpose: shortening the distance from lab to life. You ll work alongside the brightest minds to create better, faster, smarter processes to speed therapies to patients that need them the most. In fact, in a recent five-year period, INC Research/inVentiv Health has helped to develop or commercialize at least 82% of novel new drugs approved by the FDA and at least 70% of products granted marketing authorization by the EMA

Name of the Post : Clinical Trial Assistant – (17004914)

Primary Location : Asia Pacific – India, Mumbai


  • Provide (cross functional) clerical and administrative support to project team(s). In some regions this may include support to the Office Head for e.g. meeting organization, vendor management of local office issues, etc.
  • Set-up and maintain project files and investigator files
  • Fax, photocopy, and distribute study-related documents
  • Contact study personnel at sites regarding (administrative) issues
  • Order and distribute office and study related supplies needed by project team
  • Generate, maintain and distribute study-specific reports (e.g. patient enrollment, regulatory documents, site visits, investigator payments)
  • Ship/ mail supplies and documents to clients, investigator sites, and Institutional Review Boards (IRB)
  • Assist in assembling materials and binders for investigators’ meetings
  • Prepare regulatory binders (Study File Notebooks) for study sites
  • Maintain investigator payment documentation
  • When allocated by study management, collection and preparation of essential/ required documents for submission to a central IRB or a country’s central Ethics Committee, and if necessary based on local requirements the Competent Authority
  • Set up, maintain and review regulatory and administrative documents for the Trial Master File (TMF)
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  • Minimum Bachelor’s Degree, preferably from clinical / life science qualification
  • Should have 2-4 Years’ experience in Clinical Monitoring, Clinical Operation or related field
  • Good knowledge on ICH – GCP guidelines
  • Must demonstrate good computer skills especially in the utilization of Microsoft Word,
  • Excel, Power Point and analytical software
    Ready To travel if required
  • Excellent communication & interpersonal skills

Apply Online

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    • Dear Isha,

      We at Biotecnika so not schedule interviews for INC Research. Please click on the Apply Online link to be redirected to the company website where you can complete your application process.

      All the best!

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