Senior Scientific Content Developer

1 day ago


Thiruvananthapuram, Kerala, India beBeeClinical Full time ₹ 45,00,000 - ₹ 90,00,000

Key Clinical Document Specialist Role

We are seeking a highly skilled professional to develop high-quality clinical trial documents and translate complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.

  • Main Responsibilities:
  • Develop 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, well-structured documents that meet regulatory requirements and contribute to the success of clinical research and submissions.
  • Deliver accurate, timely, and effective documentation that aligns with study objectives and design.
  • Prepare and review Standard Operating Procedures (SOPs) and other relevant documents.
  • Collaborate with stakeholders to ensure comprehensive and accurate documentation within project timelines.


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