Quality solution for your company
  • Expanding Provider

    Of Industrial Solutions

  • Global Certificate

    ISO 9001:2015

  • Award Winning

    Solution Of The Year

  • Expanding Provider

    Of Industrial Solutions

  • Global Certificate

    ISO 9001:2015

  • Award Winning

    Solution Of The Year

Medical Writer

550

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Medical Writer 

Experienced Medical Writing Professionals at Clinron can design and write a wide range of high quality clinical trial documents in your style / format, efficiently within the prescribed timelines. The department has the experience necessary to deal with the unique challenges of a clinical trial; our medical writing services span across all departments, assimilating information from a wide range of expertise.

This position entails the generation of well-structured individual writers to extensively write medical writing
programs, including:

Responsibilities include –

  • üSAE Narratives (CSR, DSMBs etc.)
  • Clinical Study Protocols
  • Clinical Study Reports (ICH-E3)
  • IND Annual Reports (21 CFR 312.33)
  • Clinical Summaries/Product Feasibility Reports for Medical Devices
  • Manuscripts and Publications
  • Patient Diary Cards (PDC)
  • Informed Consent Form (ICF)
  • Subject Information Sheet (SIS)
  • Case Report Forms (CRFs)
  • Investigator Brochure
  • Protocol Case Report Form
  • Patient information leaflets
  • Informed Consent Form
  • Safety data reports
  • Medical translation services
  • Study related Forms and LogsWe can assist you with:Protocol Development, designing of Screening Form and CRF:
    Expert review and reports of Safety data:
    Statistical Analysis and Report.