GSK Hiring Clinical Compliance & Improvement Associate | GCP & Audit Readiness Role
🏢 About GSK
GSK is a global biopharmaceutical leader committed to improving global health through innovative medicines and vaccines. The company conducts clinical research across oncology, immunology, respiratory, HIV, and infectious diseases.
The Clinical Compliance & Improvement (CCI) team ensures patient safety, data integrity, and regulatory compliance across global clinical trials.
📌 Job Overview
Position: Clinical Compliance & Improvement Associate
Location: Bangalore (Hybrid – 2–3 days/week)
Additional Locations: Warsaw & Stevenage (UK)
Experience: 1–5 Years
Last Date to Apply: 6 March 2026
🔬 Role Summary
This role supports compliance monitoring, audit readiness, and continuous improvement initiatives to ensure Good Clinical Practice (GCP) compliance across global clinical programs.
If you want to strengthen your understanding of clinical data and compliance workflows, try this Clinical SAS Quiz to understand clinical datasets and regulatory documentation flow.
Professionals involved in safety oversight can also explore this Drug Safety Analyst Quiz to strengthen knowledge of safety and compliance processes.
🧾 Key Responsibilities
- Support compliance monitoring across clinical teams
- Detect operational risks and compliance trends
- Analyze compliance data to identify process gaps
- Track and verify CAPA effectiveness
- Support root cause analysis & improvement plans
- Log, track & escalate compliance issues
- Prepare documentation for audits & inspections
- Assist regulatory response preparation
- Support inspection readiness & evidence management
- Participate in continuous improvement initiatives
🎓 Eligibility Criteria
- Degree in Life Sciences, Pharmacy, Nursing or Clinical Research
- 1–5 years experience in clinical operations or compliance
- Strong understanding of Good Clinical Practice (GCP)
- Experience analyzing compliance or operational data
- Fluent English communication skills
⭐ Preferred Skills
- Regulatory inspection support experience
- Familiarity with clinical quality systems & issue management tools
- Knowledge of CAPA & root cause analysis
- Veeva clinical systems familiarity
- Excel, Power BI or data analytics tools
🌍 Why Join GSK?
- Work on global clinical trials & regulatory compliance
- Hybrid work model & flexible schedule
- International collaboration exposure
- Strong compliance & quality culture
- Career growth in clinical quality & compliance
💰 Estimated Salary (India)
₹8,00,000 – ₹16,00,000 per annum
This role focuses on GCP compliance, audit readiness, and clinical quality systems. Understanding regulatory requirements and compliance workflows improves your chances of success.
0 Comments