Clinical Trial Documentation Specialist

1 day ago


Varanasi, Uttar Pradesh, India beBeeClinicalTrial Full time ₹ 30,00,000 - ₹ 50,00,000

Key Clinical Trial Documentation Specialist

Job Description:
  • Create high-quality documents for clinical trials, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).

We are seeking an experienced Key Clinical Trial Documentation Specialist to join our team. The ideal candidate will have a strong background in creating high-quality clinical trial documents, including protocols, IBs, ICFs, CRFs, and CSRs.

Requirements:
  1. Proficient in developing key clinical trial documents.
  2. Strong scientific writing and communication skills.
  3. Ability to work independently and as part of a team.

As a Key Clinical Trial Documentation Specialist, you will be responsible for creating high-quality documents that support the success of clinical research and regulatory submissions. This is a critical role that requires attention to detail, excellent writing skills, and the ability to work effectively with cross-functional teams.

Benefits:
  • Opportunity to work on high-profile clinical trials.
  • Collaborative and dynamic work environment.
  • Professional development opportunities.

If you are a skilled writer with experience in creating clinical trial documents, we encourage you to apply for this exciting opportunity.



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