Research Document Specialist

1 day ago

Bengaluru, Karnataka, India beBeeClinical Full time US$ 65,432 - US$ 1,23,456
About the Role

We are seeking a skilled Clinical Document Author to join our team.

This individual will be responsible for authoring and analyzing clinical trial documents, working with key clinical documents including protocols, informed consent forms, and clinical study reports.

The ideal candidate will have experience in clinical research or a related field and possess strong knowledge of clinical trial phases, study design, and drug development.

  • Key Responsibilities:
  • Create, validate, and refine prompts for AI-assisted document generation.
  • Maintain compliance with global regulatory standards.
  • 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.
Requirements

To be successful in this role, you will need:

  • A minimum of 1-5 years of experience in clinical research or a related field.

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