Medical Writing Job at GSK
Experienced professionals searching for a senior-level Medical Writing Job can explore this Director Medical Writing Asset Lead opportunity at GSK in Bengaluru. This full-time, hybrid position focuses on developing medical writing strategies, leading clinical document planning, and delivering complex global regulatory submissions, primarily within Hepatology. Professionals exploring GSK Careers, Regulatory Writing Jobs, and Pharma Jobs India with substantial pharmaceutical regulatory writing experience can consider this leadership opportunity.
About GSK:
GSK is a global biopharma company focused on developing vaccines and speciality medicines using science, technology, and research. The organisation operates across multiple therapeutic areas and supports the development of medicines from clinical research through regulatory submission. This Director-level position provides experienced medical writers with an opportunity to influence clinical document strategy and global regulatory deliverables within GSK’s drug-development environment.
Job Details:
- Position: Director Medical Writing Asset Lead
- Location: Bengaluru, India
- Category: Medical and Clinical
- Job ID: 446143
- Employment Type: Full-time
- Work Model: Hybrid – Remote & On-site
- Posted On: 04 September 2026
- Primary Therapy Area: Hepatology
Job Description:
As the Director Medical Writing Asset Lead, the selected candidate will leverage their scientific and operational expertise to develop medical writing strategies for one or more assets, primarily focusing on Hepatology. This role involves designing and delivering high-quality clinical documents for global regulatory submissions and contributing to process improvements within the organisation.
Key Responsibilities:
- Providing key contributions to clinical document strategy throughout the drug development lifecycle.
- Leading matrix teams in the planning and production of clinical documents.
- Successfully delivering large submissions and recommending innovative methods for accelerated timelines.
- Acting as lead author on submissions, organising content in complex clinical documents.
- Proposing resourcing solutions for major projects.
- Contributing to the development of training materials and providing mentoring on regulatory requirements.
- Driving organisational process improvement initiatives.
- Promoting leadership behaviours that align with GSK values.
Eligibility Criteria for this Medical Writing Job:
Basic Qualifications:
- PhD, PharmD, MPH, MSc, or other post-graduate degree.
- Substantial experience in clinical regulatory writing and regulatory submissions in the pharmaceutical industry.
- Strong experience in project management and demonstrated matrix leadership.
Preferred Qualifications:
- Experience in delivering accelerated submissions for various global markets.
- Experience in the Hepatology therapy area.
- Effective communication skills and experience in building networks within the organisation.
- Excellent understanding of clinical operations and global regulatory guidelines.
- Strong strategic and critical thinking capabilities.
Skills Required for this Medical Writing Job:
- Exceptional written and verbal communication skills.
- Strong organisational and project management abilities.
- Proficiency in regulatory writing and documentation tools.
- Ability to lead and motivate cross-functional teams.
- Analytical and strategic problem-solving skills.
