Clinical Research Documentation Specialist

4 days ago


Anantapur, Andhra Pradesh, India beBeeClinicalResearch Full time ₹ 9,00,000 - ₹ 15,60,000

Job Title: Clinical Research Documentation Specialist

Looking for a skilled Clinical Research Documentation Specialist to join our team. The ideal candidate will have experience in developing high-quality clinical trial documents, including protocols, Investigator's Brochures (IBs), Informed Consent Forms (ICFs), Case Report Forms (CRFs), and Clinical Study Reports (CSRs).

  • Key Responsibilities:
  1. Developing high-quality clinical trial documents.
  2. Translating complex scientific data into clear, regulatory compliant documents.
  3. Preparing protocols, CSRs, PIS-ICFs, and CRFs.
  4. Designing the protocol based on study objectives.
  5. Reviewing and preparing SOPs.
  6. Communicating with stakeholders to ensure effective documentation within timelines.

Requirements:

  • Proficient in MS Office and Adobe Acrobat.
  • Strong understanding of clinical research regulations.
  • Excellent writing, communication, and organizational skills.

Benefits:

  • Competitive salary and benefits package.
  • Opportunity to work with a dynamic team.
  • Professional growth and development opportunities.


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