Medical/Scientific Writer-Gurgaon-AM
WNS Global Services · India
Medical Writing
Remote
physician
Pharmacist
Nurse
Demand76
Career growth66
Healthcare fit72
Remote potential32
5-year outlook
Stable demand for experienced medical writers in pharma services, but growth may be moderated by AI-assisted drafting tools; compensation typically tracks agency/CRO bands and therapeutic-area expertise rather than clinical seniority.
Clinical license
Not required
Applicant reach
moderate
Seniority
mid
Employment type
full-time
Date found
2026-11-08
Intelligence details
Flexible work details
- Engagement type
- Permanent
- Hours
- Full-time
- Profession fit
- physician, Pharmacist, Nurse
- Rate period
- Annual
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth considering if you already have writing samples, publications, or medical communications exposure and want a structured entry into industry medical affairs. Clinicians without a writing portfolio will likely be screened out by the 4-year experience bar.
Who should apply
Physicians, pharmacists, or life-science graduates with prior medical writing, publication, or medical communications experience; clinician-researchers with a strong publication record and familiarity with GPP3/ICMJE and ICH-GCP; IMGs seeking an industry-side writing career in India or globally.
CV angle
Reframe real clinical experience into evidence-communication language: highlight case reports, protocols, guideline summaries, grand-round presentations, patient education materials, audit/QI reports, and any peer-reviewed publications. Quantify deliverables (number of manuscripts, posters, educational decks) and explicitly reference familiarity with GPP3, ICMJE, and ICH-GCP. Emphasise literature appraisal, data extraction from trial databases, and cross-functional review experience rather than listing clinical duties.
Skills to highlight
- Scientific and medical writing
- Literature search and systematic review
- Manuscript and abstract preparation
- Regulatory document writing (CSR, IB, ICF)
- ICH-GCP and publication ethics (GPP3/ICMJE)
- Clinical data interpretation and synthesis
- Project and timeline management
- Stakeholder and client communication
Role summary
A mid-level medical writer role in WNS's Medical Affairs team producing scientific and regulatory content — manuscripts, abstracts, congress materials, clinical study reports, and patient/HCP education — for pharma and biotech clients, with responsibility for literature review, compliance, project delivery, and client communication.
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