Job Title: Medical Writer Total Experience - 3+years in corporate sector
Department: Medical Affairs / Scientific Communications
Education: MBBS / BDS /MDS
To develop high-quality scientific content and documentation across therapeutic areas by conducting in-depth literature reviews, synthesizing data, and delivering clear, accurate, and audience-appropriate materials.
The role involves contributing to both short- and long-term projects in the consumer healthcare and pharmaceutical sectors, including medical, safety, pre-clinical, clinical, regulatory, educational, and promotional content.
Additional responsibilities include editing, proofreading, reviewing, referencing, and verifying content to ensure adherence to high medical writing standards.
The role ensures timely delivery of project milestones while maintaining quality, compliance, and business value.
Conduct comprehensive secondary research/literature reviews and prepare overarching summaries using effective search strategies across scientific databases (e.g., Analyze and interpret clinical and scientific data to extract actionable insights.
Stay current with trends, treatment guidelines, and regulatory updates in both OTC and Rx domains.
Medical and Scientific Content Development
Leverage scientific expertise to create high-quality communication materials in the OTC and Rx space.
Research, write, edit, organize, interpret, curate, and quality-check various types of scientific content across multiple formats and channels.
Prepare, review, and edit a range of scientific documents, including:
Abstracts, posters, and slide decks for scientific conferences
Ensure scientific accuracy, clarity, and compliance with applicable guidelines (e.g., Content Review and Quality Assurance
Review medical, promotional, and scientific materials in accordance with internal SOPs and external guidelines.




Verify references and ensure content is plagiarism-free.
Ensure clear, factual, and effective presentation of data and discussions.
Project Execution
Understand and define client requirements during project initiation, including objectives and timelines.
Develop scientifically accurate and medically relevant content across therapeutic areas, adhering to branding and regulatory guidelines.
Manage multiple projects simultaneously, ensuring quality and client satisfaction.
Respond to and deliver ad-hoc client requests within agreed timelines.
Collaborate with medical writing colleagues, the graphics team, and clients as needed.
Identify learning and development needs in collaboration with the line manager and pursue relevant training opportunities.
Key Performance Indicators
Efficiency: Develop effective search strategies, organize data for analysis, and prepare medical and scientific content.
Validate sources, identify data gaps, and ensure scientific rigor.
Quality: Actively participate in team meetings, knowledge-sharing sessions, and training initiatives.
Strong understanding of the pharmaceutical, OTC, and consumer healthcare landscape.
Explicit grasp of medical, scientific, and statistical terminology and concepts.
Robust knowledge of various types of clinical studies, the structure, and formats of different manuscript types (e.g., SLR, TLR, Meta-analysis), along with their relevance and application in evidence synthesis and utilization.
Proven experience in scientific writing and literature analysis.
Proficiency in MS Office Suite (Word, PowerPoint, Excel) and online research tools.
Familiarity with regulatory documentation and compliance in US/EU markets.
Exposure to text mining, data visualization tools, and scientific storytelling.
Experience with reference management (e.g., RevMan, SPSS, GraphPad Prism, R, SAS) tools.

📌 Remote Senior Medical Writer (Gurugram)
🏢 WNS
📍 Gurugram