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Editor AI

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Onsite

Editor AI

Excelra

Editor AI

Skills

AICompliance

13 days ago

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Important information


Contract type:

Permanent

Location:

Hyderabad, Telangana, India

Work mode:

Onsite

Published on:

13 October 2026

What they need


Roles and Responsibilities :

  • Review and edit clinical trial reports, protocols, and other documents to ensure accuracy, completeness, and compliance with regulatory requirements.
  • Collaborate with cross-functional teams to develop high-quality scientific content for pharmaceutical companies.
  • Conduct thorough research on various medical topics to stay up-to-date on industry trends and best practices.
  • Ensure all edited materials meet client expectations by providing timely feedback and revisions.

Job Requirements :

  • 5-8 years of experience in medical writing or editing for the pharmaceutical industry.
  • Strong understanding of clinical trials, drug development processes, and regulations (e.g., FDA guidelines).
  • Excellent written communication skills with ability to adapt tone and style according to audience needs.
  • Proficiency in using electronic health records systems (EHRs) or similar software.

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