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    Job · 21184115

    HYDERABAD · FULLTIME

    Editor AI

    Excelra

    Excelra

    Hyderabad · onsite · Posted 5d ago

    Sourced fromNaukri
    Undisclosed5–8 yrsfulltimeHyderabad

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    Section · 01

    About this role

    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.

    Sourced from naukri

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    Section · 02

    Skills

    editor aimedical writingPharma

    Section · Company

    About Excelra

    Excelra

    Excelra

    About

    Excelra Knowledge Solutions Private Limited

    Employee ratings

    97 reviews

    3.5/ 5

    Culture

    3.5

    Career growth

    2.6

    Work-life

    3.7

    Employees rate it well for

    Salary11Work Culture8Work Life Balance8Job Security6Work Environment6

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