Senior Clinical Document Specialist

4 days ago


Vizag, Andhra Pradesh, India beBeeClinicalContentSpecialist Full time ₹ 90,00,000 - ₹ 1,20,00,000

We are seeking a skilled Clinical Content Specialist to join our team.

  • Key Responsibilities:
  •     Develop 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).
  •     Translate complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.
  •     Craft abstracts and manuscripts, demonstrating strong scientific communication skills.
  •     Deliver high-quality, accurate, and well-structured documents that contribute to the success of clinical research and regulatory submissions.
  •     Prepare protocols, CSRs, PIS-ICFs, and CRFs.
  •     Understand study objectives and design protocols.
  •     Review SOPs and communicate with stakeholders to ensure effective documentation within timelines.


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