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Medical Writer

1-3 years
preferred by company
Navi Mumbai, India
1 May 13, 2026
Job Description
Job Type: Full Time Education: M.Pharm/B.Pharm or M.Sc. Skills: Continual Improvement Process, Master Data, Material Requirements Planning (Mrp), Materials Management, People Management, Production Planning, Supplier Relationship Management (Srm), Supply-Chain Man, CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management

Job Title: Medical Writer

Company: CLINEXEL
Location: Navi Mumbai, India
Work Mode: Work From Office
Employment Type: Full-Time
Industry: Clinical Research / CRO / Medical Writing / Pharmaceutical Communications / Regulatory Writing

Job Overview

CLINEXEL is hiring a Medical Writer for its Navi Mumbai office. This role is ideal for professionals with 1–3 years of experience in medical writing, clinical research, pharmaceutical communications, biotechnology, or healthcare scientific documentation.

The role focuses on transforming complex scientific and clinical information into clear, compliant, accurate, and impactful scientific communication that supports global clinical development programs.

This opportunity is well-suited for candidates who enjoy scientific storytelling, evidence-based writing, publication development, regulatory documentation, and medical communications.


Key Responsibilities

Medical & Scientific Writing

Develop high-quality scientific content across multiple document types including:

  • Clinical study protocols
  • Clinical Study Reports (CSRs)
  • Regulatory submission documents
  • Investigator-facing documents
  • Medical/scientific manuscripts
  • Peer-reviewed publications
  • Scientific articles
  • Medical blogs
  • Evidence summaries
  • Literature reviews
  • Slide decks
  • Conference abstracts
  • Posters
  • Congress presentation materials

Regulatory Writing

Support development of compliant regulatory documentation aligned with global clinical development expectations.

Document types may include:

  • Clinical protocols
  • CSRs
  • Safety documentation
  • Submission support documents
  • Regulatory summaries

Required knowledge:

  • Regulatory writing standards
  • Documentation structure
  • Submission expectations

Publication Writing

Contribute to publication development including:

  • Manuscripts
  • Scientific papers
  • Journal-ready content
  • Conference abstracts
  • Posters
  • Publication support documents

Knowledge required:

  • Publication writing standards
  • Referencing accuracy
  • Scientific evidence presentation

Literature Review & Evidence Synthesis

  • Conduct structured literature reviews
  • Evaluate scientific evidence
  • Summarize research findings
  • Build evidence-based narratives
  • Support medical communication projects

Scientific Communication

Translate complex clinical and scientific concepts into:

  • Clear
  • Scientifically accurate
  • Audience-appropriate
  • Engaging communication

Balance scientific depth with readability.


Quality & Compliance

Ensure all deliverables meet standards for:

  • Scientific accuracy
  • Consistency
  • Structure
  • Grammar
  • Referencing
  • Compliance
  • Formatting quality

Maintain high documentation quality standards.


Cross-Functional Collaboration

Work with:

  • Clinical research teams
  • Medical teams
  • Regulatory stakeholders
  • Scientific reviewers
  • Publication contributors
  • Internal project teams

Support end-to-end content development.


Required Qualifications

Education

Preferred educational backgrounds:

  • Pharmacy
  • Life Sciences
  • Biotechnology
  • Biomedical Sciences
  • Medicine
  • Clinical Research
  • Related healthcare/scientific disciplines

Experience Required

1–3 years of relevant experience

Preferred industries:

  • Clinical research
  • CRO
  • Pharmaceuticals
  • Biotechnology
  • Healthcare communication
  • Medical communications

Required Skills

Scientific Writing Skills

  • Medical writing
  • Scientific writing
  • Regulatory writing
  • Publication writing
  • Evidence synthesis
  • Literature review

Domain Knowledge

  • Clinical research
  • Pharma development
  • Biotechnology
  • Healthcare communications
  • Drug development lifecycle

Technical Knowledge

  • Publication guidelines
  • Regulatory writing standards
  • Referencing styles
  • Scientific documentation practices

Core Competencies

  • Attention to detail
  • Scientific accuracy
  • Analytical thinking
  • Content structuring
  • Collaboration
  • Ownership mindset
  • Curiosity
  • Communication skills

What CLINEXEL Values

The company is specifically looking for candidates with:
✔ Strong scientific and medical understanding
✔ Clinical/pharma/biotech exposure
✔ Ability to simplify science without losing accuracy
✔ Publication and regulatory writing knowledge
✔ High attention to detail
✔ Structured scientific thinking
✔ Referencing discipline
✔ Ownership and accountability
✔ Collaborative mindset


Best Fit For

Candidates who can confidently work across:

  • Clinical protocols
  • CSRs
  • Regulatory documentation
  • Scientific publications
  • Literature reviews
  • Medical articles
  • Conference materials
  • Scientific presentations

Application Details

Location: Navi Mumbai
Work Mode: Office-based
Apply via email: careers@clinexel-cro.com