Manuscript Writer

1 week ago

Bengaluru, Karnataka, India MS CLINICAL RESEARCH Full time ₹ 4,00,000 - ₹ 8,00,000 per year

Job Title:
Manuscript Writer

Company:
MS Clinical Research Pvt. Ltd.

Location:
Bangalore

Job Type:
Full-time |
Immediate Joiner Preferred

Experience:
2–4 years in scientific or clinical manuscript writing and publishing

About MS Clinical Research

MS Clinical Research (MSCR) is a leading clinical research organization committed to advancing scientific innovation and improving healthcare outcomes. We conduct high-quality clinical trials that adhere to global standards of excellence and contribute to the development of breakthrough medical solutions

Job Summary

We are seeking an experienced
Manuscript Writer
with a proven track record in preparing and publishing scientific manuscripts. The ideal candidate will have strong scientific acumen, excellent writing and editing skills, and familiarity with journal publication standards. This role requires someone who can work independently, manage multiple projects, and meet tight deadlines.

Key Responsibilities

  • Develop, write, and edit scientific manuscripts, abstracts, and review articles for peer-reviewed journals.
  • Collaborate with clinical and research teams to interpret study data and present it accurately and effectively.
  • Ensure manuscripts adhere to journal-specific formatting, referencing, and submission guidelines.
  • Conduct literature searches and maintain awareness of current trends in clinical and scientific writing.
  • Prepare cover letters, responses to reviewers, and other publication-related documents.
  • Coordinate with investigators, co-authors, and journal editors during the manuscript submission and review process.
  • Maintain high scientific and ethical standards in writing and data presentation.

Qualifications

  • Bachelor's or Master's degree in Life Sciences, Pharmacy, Biotechnology, or related fields.
  • 2–4 years of hands-on experience in manuscript writing and scientific publishing (preferably in a CRO, pharma, or research organization).
  • Strong understanding of medical and scientific terminology and data interpretation.
  • Experience in handling peer-reviewed journal submissions and responding to reviewer comments.
  • Excellent command of written English and attention to detail.
  • Ability to work under tight timelines and manage multiple projects simultaneously.
  • Proficiency in MS Office and referencing tools (e.g., EndNote, Mendeley).

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