GSK has announced two high-impact openings in Bengaluru:

• Transparency Specialist – Document Anonymisation
• Regulatory Global Submission Manager

These roles are ideal for experienced professionals in clinical research, regulatory affairs, data transparency, document anonymisation, and submission management. Both positions offer excellent global exposure, cross-functional collaboration, and career-accelerating opportunities within one of the world’s most respected biopharma companies.

If you’re aiming for a long-term career in clinical data transparency, regulatory submissions, or pharmaceutical compliance, these GSK roles are among the most attractive opportunities in 2025.

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1. Transparency Specialist – Document Anonymisation (GSK, Bengaluru)

Key Responsibilities

• Lead document anonymisation activities for global transparency needs.
• Ensure compliance with EMA Policy 0070, Health Canada PRCI, and other regulations.
• Act as SME for anonymisation regulations and best practices.
• Manage vendor relationships and ensure timely document delivery.
• Oversee standard procedures, governance, and internal readiness for audits/inspections.
• Guide clinical teams on minimising PII and CCI in documents.
• Create and lead internal communities of practice to promote transparency standards.
• Monitor new technologies, tools, and approaches in document anonymisation.

Basic Qualifications

• Master’s degree in Life Sciences, Pharmacy, Clinical Research, or related field.
• 6–9 years of experience in document anonymisation or clinical transparency.
• Strong understanding of clinical trial lifecycle, metadata, and clinical documents.
• Experience in pharmaceutical matrix environments.

Preferred Skills

• Expertise in patient data handling and anonymisation practices.
• Strong communication skills across scientific and non-scientific teams.
• Experience with clinical document review, risk assessment, and process improvement.
• Ability to manage high-pressure timelines with minimal supervision.

What Success Looks Like

• Consistent on-time delivery of anonymised documents.
• Strong vendor relationships and optimized processes.
• Clear contributions to GSK’s data transparency and regulatory compliance culture.

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2. Regulatory Global Submission Manager (GSK, Bengaluru)

Key Responsibilities

• Drive global submission planning, timelines, and compliance across US, EU & ROW markets.
• Conduct critical path analysis, scenario planning, and risk mitigation.
• Manage submission content plans using RegVault & Smartsheet.
• Lead submission planning meetings and resolve blockers across functions.
• Collaborate with publishing teams for timely eCTD dossier dispatch.
• Provide regulatory guidance based on evolving global requirements.
• Manage multiple major submissions simultaneously.

Required Experience

• Hands-on experience in submission planning and lifecycle management.
• Solid understanding of global regulatory procedures (NCE/NBE, major LEs).
• Proficiency in Smartsheet, MS Project, and regulatory systems.
• Ability to work independently and influence cross-functional teams.

Preferred Skills

• Strong communication, documentation, and stakeholder management abilities.
• Experience interacting with regulatory agencies.
• Flexible mindset to meet shifting priorities and timelines.

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Benefits of Working at GSK

• Work with a globally recognized biopharma leader.
• Opportunities for professional growth and global regulatory exposure.
• Culture focused on patients, innovation, and ethical transparency.
• Inclusive work environment supporting diversity and development.

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How to Apply

Application Link for Regulatory Global Submission Manager

Application Link for Transparency Specialist Document Anonymisation