Company Description
WNS (Holdings) Limited (NYSE: WNS), is a leading Business Process Management (BPM) company. We combine our deep industry knowledge with technology and analytics expertise to co-create innovative, digital-led transformational solutions with clients across 10 industries. We enable businesses in Travel, Insurance, Banking and Financial Services, Manufacturing, Retail and Consumer Packaged Goods, Shipping and Logistics, Healthcare, and Utilities to re-imagine their digital future and transform their outcomes with operational excellence.We deliver an entire spectrum of BPM services in finance and accounting, procurement, customer interaction services and human resources leveraging collaborative models that are tailored to address the unique business challenges of each client. We co-create and execute the future vision of 400+ clients with the help of our 44,000+ employees.Position OverviewWe 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 contentProject 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 callsLiterature 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 intelligenceQuality 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 proceduresClient 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
Required QualificationsEducation: 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.PreferredVeeva experience, therapeutic expertise (oncology, immunology, metabolic disorders), creative designing, HEOR knowledge, team mentoring experience.
