Medical and Scientific Writer

WNS Global Services Pvt Ltd; Gurugram District; On-site; INR 1,800,000 - 2,400,000; Full time

Job summary

WNS Global Services Pvt Ltd, Gurgaon, seeks an experienced Medical Writer to join its Medical Affairs team. The role focuses on developing high-quality scientific content across therapeutic areas for pharmaceutical and biotechnology clients, translating complex clinical data into clear, compliant communications for diverse stakeholders.

You will manage multiple projects, ensure regulatory alignment (FDA, EMA, ICH-GCP), and contribute to publications, regulatory documents, and educational

Qualifications

• Advanced degree in life sciences or related field; PhD/PharmD/MD/MS
• Minimum 4 years in medical writing with demonstrable deliverables
• Ability to translate clinical data into compliant communications
• Experience with regulatory documents and publications
• Familiarity with FDA, EMA, ICH-GCP guidelines

Responsibilities

• Develop scientific content across therapeutic areas for pharma/biotech clients
• Prepare regulatory documents such as clinical study reports and brochures
• Create publications for peer-reviewed journals per guidelines
• Coordinate cross-functional reviews with medical, regulatory, and commercial teams
• Manage multiple projects, timelines, and budgets with quality standards

Skills

Advanced scientific writing

Project management

Excellent communication

Clinical trial databases knowledge

Literature search

Education

PhD in life sciences

PharmD

MD

MS

Bachelor's degree

Tools

Microsoft Office

Reference management software

Job description

Medical/Scientific Writer-Gurgaon-AM Company Description WNS, part of Capgemini, is an Agentic AI-powered leader in intelligent operations and transformation, serving more than 700 clients across 10 industries, including Banking and Financial Services, Healthcare, Insurance, Shipping and Logistics, and Travel and Hospitality. We bring together deep domain excellence - WNS' core differentiator - with AI-powered platforms and analytics to help businesses innovate, scale, adapt and build resilience in a world defined by disruption.Our purpose is clear: to enable lasting business value by designing intelligent, human-led solutions that deliver sustainable outcomes and a differentiated impact. With three global headquarters across four continents, operations in 13 countries, 65 delivery centers and more than 66,000 employees, WNS combines scale, expertise and execution to create meaningful, measurable impact.

Job Description

Position Overview

We are seeking an experienced Medical Writer to join our Medical Affairs team.

The ideal candidate will develop high-quality scientific content across diverse therapeutic areas for pharmaceutical and biotechnology clients.

This role requires strong scientific writing skills, attention to detail, and the ability to translate complex clinical data into clear, compliant communications for various stakeholders.

Key Responsibilities

Scientific Content Development

• Develop and coordinate medical communications deliverables including slide decks, congress materials, manuscripts, abstracts, posters, and advisory board presentations
• Prepare regulatory documents such as clinical study reports, investigator brochures, and informed consent forms
• Create publications for peer-reviewed journals following GPP3/ICMJE guidelines
• Develop educational materials for healthcare professionals and patient-focused content

Project Management

• Manage multiple projects simultaneously while meeting tight deadlines and quality standards
• Coordinate cross-functional reviews with medical, regulatory, and commercial stakeholders
• Track project timelines, budgets, and deliverables using project management tools
• Participate in client meetings and status update calls

Literature and Data Analysis

• Conduct comprehensive literature searches and data extraction from clinical trial databases
• Synthesize scientific data from clinical studies, meta-analyses, and systematic literature reviews
• Ensure accuracy and consistency of scientific content with source documents
• Maintain awareness of current therapeutic landscape and competitive intelligence

Quality and Compliance

• Ensure all content adheres to regulatory guidelines (FDA, EMA, ICH-GCP)
• Implement client style guides, brand guidelines, and standard operating procedures
• Participate in quality control processes and peer review activities
• Maintain document version control and archival procedures

Client Relationship Management

• Build and maintain strong client relationships through responsive communication
• Understand client needs and provide strategic recommendations
• Contribute to proposal development and scoping activities
• Support new business development initiatives

Qualifications

Education

Advanced degree (PhD, PharmD, MD, MS) in life sciences, pharmacy, medicine, or related field. Bachelor's with exceptional experience considered.

Experience

Minimum 4 years in medical writing (pharmaceutical industry, CRO, or medical communications agency) with proven deliverables across publications, regulatory documents, and congress materials.

Skills

• Expert medical writing
• Microsoft Office proficiency
• Reference management software
• Clinical trial databases knowledge
• Strong project management
• Excellent communication

Preferred Veeva experience, therapeutic expertise (oncology, immunology, metabolic disorders), creative designing, HEOR knowledge, team mentoring experience.