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Document Specialist for Pharmaceutical Industry

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Mount Abu, Rajasthan, India beBeeClinicalResearch Full time ₹ 9,00,000 - ₹ 12,00,000
Clinical Research Document Specialist

As a Clinical Research Document Specialist, you will play a pivotal role in developing high-quality clinical trial documents that support drug development and approval processes.

  • We are seeking an experienced professional to join our team in creating key clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).
  • The ideal candidate will have a strong background in translating complex scientific data into clear, regulatory compliant documents.
  • Your responsibilities will include:
    • Developing high-quality clinical trial documents
    • Translating complex scientific data into clear, regulatory compliant documents
    • Crafting abstracts and manuscripts
    • Delivering high-quality, accurate, and well-structured documents
  • You will be responsible for communicating with all stakeholders to ensure effective and complete documentation within the timeline.
  • In addition, you will be expected to prepare and review SOPs, understand study objectives, and design protocols.