Medical Writing Job at GSK | Apply Now
Looking for a high-impact medical writing job in a global biopharma leader? This opportunity at GSK offers experienced professionals the chance to lead oncology medical writing strategies across global markets. If you are exploring GSK careers, this role combines scientific expertise, leadership, and innovation to shape regulatory submissions and improve patient outcomes worldwide. Discover how this medicine job can elevate your career in one of the top medical jobs in Bangalore and beyond.
Job Details
- Job Position: Director Medical Writing Asset Lead, Oncology
- Job ID: 435813
- Location: GSK HQ, Bangalore
- Job Type: Full-Time
- Department: Medical and Clinical
- Application Deadline: 13th April 2026
About the Company
GSK is a global biopharma company with a purpose to unite science, technology, and talent to get ahead of disease together. The company aims to positively impact the health of 2.5 billion people by the end of the decade.
GSK focuses on discovering and delivering vaccines and medicines by combining its understanding of the immune system with cutting-edge technology. The organization emphasizes innovation across therapeutic areas such as respiratory, immunology and inflammation, oncology, HIV, and infectious diseases. With a strong culture built on ambition for patients, accountability for impact, and doing the right thing, GSK careers offer professionals a meaningful environment to thrive and contribute to global healthcare advancements.
Job Description
This medical writing job involves leading medical writing for one or more oncology development assets, with accountability for asset-level strategy from planning to delivery.
The role is highly strategic and visible, requiring collaboration with Clinical Development, Regulatory Affairs, Biostatistics, Safety, and other cross-functional teams. You will shape regulatory strategies and deliver high-quality clinical documents for global submissions. This medicine job demands balancing scientific rigor with efficient execution, simplifying document lifecycles, and improving submission quality while reducing risk. It is an excellent opportunity within GSK careers to make a meaningful impact in global healthcare.
Qualifications
Basic
- Postgraduate degree (e.g., medicine or related discipline)
- Significant experience in clinical regulatory medical writing in pharma or biotech
- Experience in global oncology submissions (FDA and/or EMA)
- Experience managing cross-functional teams and external vendors
- Strong program management and project planning skills
- Excellent written and verbal communication skills
Preferred
- Experience with accelerated global submissions
- Mentoring and training experience
- Knowledge of global regulatory guidelines and Good Clinical Practice
- Experience with medical writing technologies and process improvements
- Experience working in global matrix organizations
Key Responsibilities
- Lead strategy, planning, authoring, and delivery of clinical documents across the asset lifecycle
- Prepare clinical study protocols, investigator brochures, clinical study reports, and regulatory submission documents
- Drive asset-level medical writing strategy aligned with global development and regulatory goals
- Lead and coach cross-functional matrix teams and external vendors
- Manage complex global submissions with accelerated timelines
- Develop submission and document lifecycle plans
- Act as lead author or senior reviewer for regulatory documents and queries
- Define resourcing strategies using internal teams and external vendors
- Improve processes, technologies, and document quality
- Mentor team members and build oncology medical writing capabilities
What Success Looks Like
- Delivering timely, high-quality global oncology submissions
- Leading innovative and accelerated submission strategies
- Strengthening internal capabilities and vendor partnerships
- Improving document lifecycle efficiency and reducing risks
- Driving excellence in this medical writing job within a global environment
