Global biopharma leader GSK is hiring a Clinical Compliance & Improvement Associate for its Development Operations team in Bangalore, India, with additional locations in Warsaw and Stevenage (UK).
If you have 1–5 years of experience in clinical operations, GCP compliance, audit readiness, or clinical quality systems, this is a strong opportunity to build a career in clinical compliance, inspection readiness, and continuous improvement within global trials.
📅 Last Date to Apply: 6 March 2026
📍 Location: Bangalore (Hybrid – 2–3 days/week office)
About the Role – Clinical Compliance & Improvement Associate
The Clinical Compliance & Improvement (CCI) team plays a critical role in ensuring:
- Patient safety
- Data integrity
- GCP compliance
- Early risk detection in clinical trials
This position supports compliance monitoring, issue governance, and audit/inspection readiness across global clinical programs.
Primary Keywords:
Clinical Compliance Associate jobs, GCP jobs in Bangalore, Clinical Quality jobs India, Pharma compliance careers 2026
Key Responsibilities
1️⃣ Compliance Monitoring & Risk Detection
- Support compliance monitoring activities across assigned clinical teams
- Detect operational risks, compliance signals, and emerging trends
- Analyze compliance data to identify process gaps
2️⃣ Corrective & Preventive Actions (CAPA)
- Assist in compliance checks and management monitoring
- Track and verify effectiveness of corrective actions
- Support root cause analysis and improvement plans
3️⃣ Issue Governance & Documentation
- Log, track, and escalate compliance issues
- Coordinate communication of actions and outcomes
- Maintain strong documentation discipline aligned with GCP
4️⃣ Audit & Inspection Readiness
- Prepare documentation for inspections and internal audits
- Assist in regulatory response preparation
- Ensure evidence readiness for regulatory authorities
5️⃣ Continuous Improvement Projects
- Support small improvement initiatives
- Use data analytics tools (Excel, Power BI, AI tools)
- Collaborate across quality, clinical, and operational teams
Eligibility Criteria
Required Qualifications
- Degree in Life Sciences / Pharmacy / Nursing / Clinical Research
- 1–5 years experience in:
- Clinical operations
- Clinical compliance
- Quality systems
- Regulatory inspection support
- Strong knowledge of Good Clinical Practice (GCP)
- Experience analyzing compliance or operational data
- Fluent English communication skills
- Comfortable working in a hybrid R&D environment
Preferred (Plus) Skills
- Experience supporting regulatory inspections
- Familiarity with:
- Clinical quality systems
- Issue management tools
- Veeva clinical systems
- Knowledge of:
- Root cause analysis
- CAPA implementation
- Study oversight processes
- Proficiency in Excel, Power BI, or data visualization tools
Why Join GSK?
Working at GSK means contributing to global clinical research across therapeutic areas including oncology, respiratory, immunology, HIV, and infectious diseases.
Benefits Include:
- Hybrid working model (2–3 days office)
- Flexible work hours
- International collaboration exposure
- Medical insurance & life coverage
- Retirement benefits
- Annual performance bonus
- Learning & development opportunities
- Strong global compliance culture
Salary Details (India – Estimated)
Based on industry benchmarks for 1–5 years experience in Bangalore:
💰 Estimated CTC Range: ₹8,00,000 – ₹16,00,000 per annum
(Final compensation depends on experience and internal grade alignment)
How to Apply
