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Junior Medical Writer And Mid-Level Medical Writer

Health Minds
1-5 years
Not Disclosed
Remote
2 June 4, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: mRS and EQ-5D-5L., Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Junior Medical Writer / Mid-Level Medical Writer

Job Title: Junior Medical Writer / Mid-Level Medical Writer
Company: HealthMinds Consulting Private Limited
Employment Type: Full-Time
Work Mode: On-Site / Remote (Project Dependent)
Shift: US Shift (5:30 PM – 3:00 AM IST)

Locations

  • Mumbai: Godrej Business District, LBS Marg, Pirojshanagar, Vikhroli West, Mumbai

  • Bengaluru: Beacon Tower, Brigade Twin Towers, Yeshwantpur, Bengaluru


About the Role

HealthMinds Consulting is seeking highly motivated Medical Writers with expertise in scientific content development, reference management, annotation, and regulatory compliance. The role involves supporting medical communications, promotional review processes, and content governance activities while ensuring scientific accuracy and adherence to global regulatory standards.

The ideal candidate should possess strong experience in medical writing, literature evaluation, referencing, ontology mapping, and MLR/PRC submission processes.


Key Responsibilities

Medical Writing & Scientific Content Development

  • Develop scientifically accurate and evidence-based medical content.

  • Conduct literature reviews and synthesize scientific information from published research.

  • Support development of:

    • Medical communication materials

    • Scientific documents

    • Promotional materials

    • Educational content

  • Ensure content aligns with scientific evidence and regulatory requirements.


Reference Tagging & Annotation

  • Perform comprehensive reference tagging and annotation activities.

  • Ensure accurate linkage between scientific claims and supporting references.

  • Maintain traceability and compliance across all deliverables.

  • Verify references for completeness, accuracy, and consistency.


Ontology Mapping & Scientific Classification

  • Conduct ontology mapping using standard medical terminologies such as:

    • MeSH (Medical Subject Headings)

    • MedDRA (Medical Dictionary for Regulatory Activities)

    • SNOMED CT

  • Ensure scientific content is categorized and mapped appropriately.

  • Support data standardization and content organization initiatives.


MLR / PRC Submission Support

  • Prepare content packages for:

    • Medical Legal Review (MLR)

    • Promotional Review Committee (PRC)

  • Ensure all materials meet submission-readiness requirements.

  • Support regulatory review processes and address reviewer feedback.


Annotation of Scientific & Promotional Materials

  • Annotate a wide range of materials, including:

    • Product Labels (LBLs)

    • Slide Decks

    • Brochures

    • Email Campaigns

    • Interactive Visual Aids (IVAs)

    • Promotional Materials

    • Scientific Presentations

  • Ensure compliance with client-specific annotation requirements and regulatory standards.


Quality Control & Compliance

  • Conduct thorough quality control reviews before final submission.

  • Perform peer reviews of scientific and promotional content.

  • Verify:

    • Reference accuracy

    • Annotation completeness

    • Regulatory compliance

    • Formatting consistency

  • Ensure adherence to:

    • AMA Referencing Style

    • Vancouver Referencing Style

    • Client-Specific Guidelines

    • Medical Governance Standards


Documentation & Tracker Management

  • Develop and maintain:

    • Reference Trackers

    • Annotation Databases

    • Submission Logs

    • Content Libraries

  • Support efficient retrieval and management of scientific references.


Cross-Functional Collaboration

  • Collaborate with:

    • Medical Writers

    • Medical Review Teams

    • Project Managers

    • Creative Teams

    • Regulatory Review Teams

  • Resolve content-related queries and ensure alignment across stakeholders.

  • Support project timelines and delivery commitments.


Process Improvement

  • Contribute to initiatives aimed at improving:

    • Annotation workflows

    • Referencing processes

    • Quality standards

    • Operational efficiency

  • Recommend best practices for scientific content management and compliance.


Required Qualifications

Education

Candidates must possess one of the following:

  • PharmD

  • M.Pharm

  • M.Sc. (Life Sciences)

  • PhD (Life Sciences)

  • Equivalent Advanced Degree in Life Sciences


Experience Requirements

Junior Medical Writer

  • 1–2 years of relevant experience in:

    • Medical Writing

    • Scientific Content Development

    • Annotation & Referencing

    • Medical Communications

Mid-Level Medical Writer

  • 3–4 years of relevant experience in:

    • Medical Writing

    • MLR/PRC Review Support

    • Annotation & Referencing

    • Medical Communications

Senior Medical Writer

  • 5+ years of relevant experience in:

    • Scientific Writing

    • Medical Communications

    • Promotional Review Support

    • Medical Governance