Medical Writer II

2 weeks ago

India Syneos Health Full time US$ 60,000 - US$ 1,00,000 per year

Job Description

  • Experience in QC of regulatory MW documents (protocols including amendments, CSRs, IBs and updates, etc).

    • Compiles, writes, edits, and coordinates medical writing deliverables that present scientific information clearly and accurately, and works as a medical writer within and across departments with minimal or moderate supervision.

    • Completes a variety of documents that may include clinical study protocols and clinical study protocol amendments; clinical study reports; patient narratives; annual reports; investigator brochures; informed consents; annual reports; plain language summaries; periodic safety update reports; journal manuscripts; and abstracts, posters, and presentations for scientific meetings.

    • Adheres to established regulatory standards, including, but not limited to, ICH E3 guidelines, as well as company standard operating procedures, client standards, and company and/or client approved-templates, authorship requirements, and style and formatting guides, when completing

    medical writing projects, on time and on budget.

    • Coordinates quality and editorial reviews. Ensures source documentation is managed appropriately. Leads document reviews, reviews documents as needed, and resolves comments from client.

    • Acts as peer reviewer for internal team to ensure document scientific content, clarity, overall consistency, and proper format.

    • Reviews statistical analysis plans and table/figure/listing specifications for appropriate content,and for grammar, format, and consistency. Provides feedback to further define statistical output required.

    • Interacts and builds good working relations with clients, department head, and peers, as necessary, to produce writing deliverables.

    • Performs online clinical literature searches and complies with copyright requirements.

    • Identifies and proposes solutions to resolve document issues, escalating as appropriate.

    • Mentors less experienced medical writers on projects, as necessary.

    • Maintains a strong working knowledge of drug development process, regulatory guidelines,industry standards, and best practices.

    • Aware of budget specifications for assigned projects, working within the budgeted hours and communicating status and changes to medical writing leadership.

    • Completes required administrative tasks within the specified timeframes.

    • Performs other work-related duties as assigned.

What we're looking for:

  • Bachelors degree in a relevant discipline with relevant writing experience; graduate degree preferred.
  • At least 2 years of relevant experience in science, technical, or medical writing.

    • Experience working in the biopharmaceutical, device, or contract research organization industry preferred.

    • Familiar with FDA and ICH regulations, other regulatory guidelines, and/or good publication practices strongly preferred.

    • Experience writing relevant document types preferred.

    • Extensive knowledge of English grammar and ability to communicate clearly; familiar with AMA Manual of Style.

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