Document Authoring Specialist

3 days ago

Nagpur, Maharashtra, India beBeeClinicalResearchAssociate Full time ₹ 90,00,000 - ₹ 1,20,00,000

About This Role:

This role is for a skilled professional who will work on authoring and analyzing clinical trial documents.

You will be responsible for creating, validating, and refining prompts for AI-assisted document generation.

Apply your knowledge of clinical trial phases, study design, and drug development to maintain compliance with global regulatory standards.

You will utilize medical terminologies and ontologies for clarity and consistency, ensuring quality control and timely delivery of assigned tasks.

Main Responsibilities:

  • Author and analyze clinical trial documents
  • Create, validate, and refine prompts for AI-assisted document generation
  • 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
  • Ensure quality control and timely delivery of assigned tasks
  • Collaborate with cross-functional teams to improve document accuracy and prompt effectiveness

Benefits:

This position offers opportunities for growth and development in a dynamic and innovative environment.

You will have the chance to work with a talented team of professionals and contribute to the success of our organization.

We are committed to providing a supportive and inclusive workplace culture.

About Us:

We are a leading provider of IT services and solutions.

Our mission is to deliver high-quality services that meet the evolving needs of our clients.

We value innovation, collaboration, and excellence in all that we do.

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