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Principal Medical Writer

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About us:

We're a global IT services company with presence in over 50 locations across more than 25 countries. Our expertise lies in digital engineering and IT services, helping clients modernize their technology infrastructure and adopt cloud and AI solutions.

Our team partners with major firms in various industries, including banking, healthcare, telecom, and media. We combine deep industry knowledge with agile development practices to deliver scalable and cost-effective digital transformation.

Job Title: Clinical Document Authoring

Key Responsibilities:

  • Author and analyze clinical trial documents.
  • Work with key clinical documents such as protocols, informed consent forms, and clinical study reports.
  • 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.
  • 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.

This role requires 1-5 years of experience and any graduation qualification. The work mode is hybrid, and the employment type is contract-based.