Apply for Director Medical Writing Oncology at GSK. Check eligibility, responsibilities, global locations, salary details and apply before deadline now today.
Introduction
Senior professionals in regulatory writing and oncology now have an exciting global opportunity. The Director Medical Writing Asset Lead Oncology at GSK role is designed for experienced leaders who can drive medical writing strategy across global clinical programs. This position offers high visibility, leadership responsibility, and the chance to contribute to innovative oncology treatments impacting patients worldwide.
Job Overview
| Job Title | Director – Medical Writing Asset Lead (Oncology) |
|---|---|
| Company Name | GSK |
| Location | Bangalore, London, Wavre, Mississauga, Siena, Stevenage, Pennsylvania, Warsaw |
| Employment Type | Full-Time |
| Department | Medical & Clinical / Oncology |
| Experience Required | Extensive (Senior-Level Role) |
| Education | PhD / PharmD / MSc / MPH / Life Sciences |
| Salary | As per company standards |
Company Overview
GSK is a leading global biopharmaceutical company focused on developing innovative medicines and vaccines. With a strong emphasis on science, technology, and patient-centric innovation, GSK aims to positively impact billions of lives. The company operates across multiple therapeutic areas, including oncology, immunology, infectious diseases, and respiratory care, offering a dynamic and growth-oriented work environment.
Job Location & Employment Type
- Locations: Bangalore (India), UK, Belgium, Canada, Italy, USA, Poland
- Employment Type: Full-Time
- Last Date to Apply: April 13, 2026
Open Positions / Department Details
This role is part of the Global Medical Writing and Oncology R&D team, responsible for developing high-quality regulatory documents for clinical development programs. The position involves working in a matrix environment with multiple global stakeholders.
Key Roles & Responsibilities
Medical Writing Leadership
- Lead planning, authoring, and delivery of clinical and regulatory documents
- Develop asset-level medical writing strategies aligned with regulatory goals
- Prepare documents such as clinical study reports, protocols, IND/IMPD sections, and CTD summaries
Regulatory & Scientific Collaboration
- Partner with Clinical Development, Regulatory Affairs, Biostatistics, and Safety teams
- Ensure clear scientific communication and regulatory compliance
- Support global submissions and responses to regulatory authorities
Project & Team Management
- Lead cross-functional teams and manage external vendors
- Ensure timely delivery of high-quality documents within budget
- Identify risks and implement mitigation strategies
Process Improvement & Innovation
- Drive efficiency in document lifecycle and submission processes
- Implement new technologies and improve writing standards
- Contribute to organizational capability building
Mentorship & Capability Development
- Train and mentor junior medical writers
- Support development of training materials and best practices
- Promote collaboration and high-performance team culture
Eligibility Criteria
Education
- Postgraduate degree (PhD, PharmD, MSc, MPH) in Life Sciences, Pharmacy, Medicine, or related field
Experience
- Significant experience in clinical regulatory medical writing
- Proven experience in oncology submissions (FDA/EMA)
- Experience leading global teams and managing vendors
Skills Required
- Strong expertise in regulatory writing and clinical documentation
- Knowledge of global regulatory guidelines and GCP principles
- Excellent communication and scientific writing skills
- Leadership and project management capabilities
- Ability to manage complex global submissions
- Strong problem-solving and strategic thinking skills
Salary & Benefits
- Salary: As per company standards (varies by location)
- Performance-based incentives and bonuses
- Global exposure and leadership opportunities
- Private healthcare, insurance, and retirement benefits (location dependent)
- Flexible working environment
- Career growth in senior leadership roles
Selection Process
The recruitment process typically includes:
- Online application submission
- Profile shortlisting
- Technical and leadership interview rounds
- HR discussion
- Final selection
How to Apply
Interested candidates can apply for the Director Medical Writing Asset Lead Oncology at GSK role through the official GSK careers portal. Submit an updated CV along with a brief cover letter highlighting your experience.
Important Dates
- Last Date to Apply: April 13, 2026
Why Apply for This Job?
- Lead global oncology medical writing strategies
- Work with one of the top biopharma companies worldwide
- Contribute to life-saving cancer therapies
- Gain exposure to international regulatory submissions
- Opportunity to mentor teams and shape organizational capabilities
- Strong career progression into executive leadership roles
FAQs
1. Who can apply for this role?
Experienced professionals with postgraduate qualifications and strong background in regulatory medical writing and oncology can apply.
2. Is oncology experience mandatory?
Yes, experience in oncology submissions and clinical development is highly preferred.
3. What is the salary range?
Salary is not disclosed and varies by country and experience level.
4. Is this a remote job?
No, this is a full-time role based in multiple global office locations.
5. How can I apply?
You can apply online through the official GSK careers website with your CV and cover letter.
Conclusion
The Director Medical Writing Asset Lead Oncology at GSK is a prestigious leadership role for experienced professionals in clinical regulatory writing. With global exposure, impactful work in oncology, and strong career advancement opportunities, this position is ideal for those aiming to lead innovation in pharmaceutical R&D. Apply before the deadline to secure your opportunity.
Disclaimer
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