Clinical Documentation Specialist

3 days ago


Vellore, Tamil Nadu, India beBeeScientific Full time ₹ 15,00,000 - ₹ 20,00,000

Medical writers and clinical study researchers play a pivotal role in the drug development process.

Key Responsibilities:
  • Develop high-quality 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 facilitate the approval of new drugs and treatments.
  • Craft compelling abstracts and manuscripts showcasing strong scientific communication skills.
  • Publish research findings in reputable journals to enhance the visibility of clinical trials and advance medical knowledge.
Requirements:
  • Proficiency in writing high-quality clinical trial documents.
  • Excellent scientific communication and presentation skills.
  • Ability to collaborate with cross-functional teams to achieve project goals.
Benefits:

As a Medical Writer/Clinical Study Researcher, you will have opportunities to work on diverse projects, develop your expertise, and contribute to the advancement of medical science.

We offer a dynamic and collaborative work environment that fosters growth, learning, and innovation.



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