PHARMAFull-time
Senior Medical Writer - Content Quality Review
BANGALORE (IN)HYBRIDPOSTED: 9/28/2026
PHARMAFull-time
HIRING ORGANIZATIONGSKPharmaceuticals / Healthcare / Life Sciences
ROLE OVERVIEW
Drive QC consistency, compliance, and scientific accuracy for complex clinical and regulatory documents at GSK.
ROLE DEFINITION & RESPONSIBILITIES
- •Perform in-depth checks of alignment between text, tables, listings, figures, and statistical outputs
- •Ensure coherent, aligned, and data-supported messages across related documents
- •Review deliverables against standard quality KPIs
- •Drive consistency of lean authoring standards, language, editorial aspects, and terminology
- •Partner with medical writers and clinical colleagues to resolve content and data issues
- •Lead and own project-level QC planning and delivery independently
- •Provide coaching to new QC reviewers and contribute to process-improvement initiatives
Reporting Hierarchy: Reports to Head of Medical Writing / Quality Control • Team size: 5-10
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Bachelor's or master's degree in Life Sciences / Pharmacy / Biomedical Sciences
- 5+ years of content QC experience in the pharmaceutical industry
- Understanding of clinical development and regulatory documents
- Knowledge of ICH / GCP
PREFERRED QUALIFICATIONS
- •Medical writing experience in patient narratives and clinical documents
- •Advanced proficiency in MS Word and document management systems
- •AI literacy and digital proficiency
REQUIRED VERIFIED SKILLS
Medical Writing
Quality Control
Clinical Research
Regulatory Documents
ICH-GCP
CSR
Protocols
Data Review
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Health insurance, PF, Paid leave, Hybrid flexibility, Professional development
Competitive compensation packages reflecting senior industry experience in pharmaceutical quality control and medical writing.
ORGANIZATION CONTEXT & CULTURE
Global biopharma company uniting science, technology, and talent to get ahead of disease.
TEAM SIZE: 70,000+ employees
INDUSTRY: Pharmaceuticals / Healthcare / Life Sciences
Culture: Ambitious for patients, accountable for impact, and committed to doing the right thing.
EXPECTED CAREER ROADMAP
Progression opportunities include Principal Medical Writer, Quality Lead, and Head of Medical Writing roles.
APPLICATION ADVISORY
Highlight your specific experience in reviewing clinical study reports (CSRs), protocols, and investigator brochures alongside your digital proficiency.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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