Senior Clinical Document Analyst

1 week ago


Guntur, Andhra Pradesh, India beBeeClinicalResearch Full time ₹ 7,50,000 - ₹ 15,00,000

About Clinical Research Associates:

We are a global firm with operations across 50+ locations worldwide, specializing in digital engineering and IT services.

We operate globally with delivery centers around the world. Our expertise combines deep industry knowledge with agile development practices.

Key Responsibilities:

  • Analyze clinical trial documents and create AI-assisted document generation prompts.
  • Work with key clinical documents: Protocol, Informed Consent Form, Clinical Study Report, Summary of Clinical Safety/Efficacy, and more.
  • Apply knowledge of clinical trial phases, study design, and drug development.
  • Maintain compliance with global regulatory standards (FDA, EMA, ICH-GCP).
  • Utilize medical terminologies and ontologies for clarity and consistency.

Requirements:

  • 1-5 years of experience.
  • Bachelor's degree or higher.

Job Benefits:

We offer opportunities for professional growth and collaboration with cross-functional teams.

Why Choose Us:

We provide regular updates and flag risks to project managers.



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