Clinical Research Document Specialist

14 hours ago


Bareilly, Uttar Pradesh, India beBeeScientific Full time ₹ 12,00,000 - ₹ 15,00,000

Overview:

  • This role focuses on creating 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).

Key Responsibilities:

  • Developing and translating complex scientific data into clear, regulatory compliant documents that support drug development and approval processes.
  • Crafting abstracts and manuscripts, demonstrating strong scientific communication skills.
  • Delivering high-quality, accurate, and well-structured documents that contribute to the success of clinical research and regulatory submissions.

Requirements:

  • Proficient in developing high-quality key clinical trial documents.
  • Strong understanding of study objectives and protocol design.
  • Excellent communication skills to ensure effective documentation within timelines.

Benefits:

  • Opportunity to work on various clinical trials and projects.
  • Challenging and rewarding work environment.
  • Chance to develop and improve clinical research skills.

Preferred Qualifications:

  • Experience in crafting abstracts and manuscripts.
  • Strong scientific knowledge and translation skills.
  • Ability to communicate effectively with stakeholders.


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