Medical Writer/ Clinical Study Researcher

5 days ago

Mumbai, Maharashtra, India MindPec Solutions Full time

Open for Delhi and Bangalore location only

  • Proficient in developing high-quality key clinical trial documents, including protocols, Investigator's Brochures (IBs)
  • Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
  • Proficient in translating complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.
  • Additionally, experienced in crafting abstracts and manuscripts, demonstrating strong scientific communication skills.
  • Committed to delivering high-quality, accurate, and well-structured documents that contribute to the success of clinical research and regulatory submissions.
  • Preparation of protocols, CSRs, PIS-ICFs and CRFs.
  • Understanding the study objectives and designing the protocol.
  • Preparation and review of SOPs.
  • Communicating with all stakeholders to ensure effective and complete documentation within the timeline.

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