Sr Medical Editor

4 - 7 years

4 - 7 Lacs

Posted:2 days ago| Platform: Foundit logo

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Work Mode

On-site

Job Type

Full Time

Job Description

Sr. Medical Editor

Roles & Responsibilities

  • Quality & Compliance Oversight:

  • Maintain familiarity with

    FDA, EU, and other relevant guidelines

    to ensure documents meet or exceed regulatory requirements.
  • Perform

    data integrity review

    of assigned documents to ensure accuracy.
  • Copyedit documents, applying correct

    grammar, punctuation, spelling, and style

    following the

    AMA (American Medical Association) style guide

    or other custom guidelines.
  • Project & Team Leadership:

  • Act as a

    project lead

    for complex and large medical writing projects.
  • Monitor timelines and budgets for assigned projects, updating relevant stakeholders if deliverables are at risk.
  • Serve as a mentor, providing technical support and training to medical editing staff.
  • Advise medical writers and study teams on

    data integrity review, compilation, and editorial standards

    .
  • Collaboration & Process Improvement:

  • Represent the editorial group on study teams and cross-departmental project teams.
  • Collaborate with the medical writing team and provide feedback on the progress of the editorial process.
  • Contribute to the development of process improvement tools and the revision of internal policies affecting editorial work.
  • May be responsible for compiling and publishing medical writing deliverables.

Qualifications

  • A Bachelor's degree (preferred) in the

    life sciences, clinical sciences, English/journalism

    , or relevant copyediting experience.
  • Strong proficiency in

    Microsoft Office Suite

    (Word, Excel, and PowerPoint).
  • Excellent

    attention to detail

    , along with strong

    copyediting, data integrity review, and problem-solving skills

    .
  • Excellent

    grammatical and communication skills

    , both written and oral.
  • Extensive familiarity with the

    AMA style guide

    is strongly preferred.
  • Proven ability to work independently with minimal supervision on multiple assignments with set deadlines.
  • Experience with publishing software like

    Adobe Acrobat

    and

    ISIToolbox

    is a plus.
  • Knowledge of

    FDA, EU, and ICH regulations

    as applicable to regulatory documents is preferred.

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