Job Title: Clinical Compliance & Improvement Associate
Locations: Warsaw, Poland | Bangalore, India | Stevenage, Hertfordshire, United Kingdom
Job Function: Medical and Clinical Operations
Job ID: 435667
Company: GSK
Job Overview
GSK is seeking a Clinical Compliance & Improvement Associate to join the Clinical Compliance & Improvement (CCI) team within Development Operations. This role supports clinical trial compliance monitoring, early risk detection, quality oversight, and continuous improvement initiatives across global clinical programs.
The position offers strong exposure to clinical operations, GCP compliance frameworks, regulatory inspection readiness, and data-driven quality improvements. You will collaborate cross-functionally with clinical, quality, and operational stakeholders to safeguard patient safety, regulatory adherence, and data integrity.
This opportunity is ideal for professionals looking to grow their career in clinical quality assurance, risk management, and trial oversight within a global biopharmaceutical environment.
Key Responsibilities
Support compliance monitoring activities to detect operational risks, trends, and emerging signals across assigned clinical teams
Conduct compliance checks, management monitoring, and follow-up assessments to verify effectiveness of corrective actions
Collect, analyze, and present compliance metrics and insights to inform quality improvement strategies
Assist in issue governance processes including logging, tracking, escalation, and communication of outcomes
Support regulatory inspection and internal audit readiness activities by preparing documentation and evidence
Contribute to continuous improvement initiatives including root cause analysis and CAPA implementation
Collaborate with cross-functional stakeholders to enhance oversight and study execution standards
Maintain alignment with Good Clinical Practice (GCP) and global regulatory expectations
Educational Qualification
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, Clinical Research, or related discipline
Equivalent relevant professional experience may be considered
Experience Required
1–5 years of experience in Clinical Operations, Clinical Quality, Compliance, or related function
Practical knowledge of Good Clinical Practice (GCP) and global clinical trial conduct
Experience analyzing operational or compliance data to identify process gaps or trends
Exposure to regulatory inspections or internal audits is preferred
Familiarity with clinical systems such as Veeva and quality management tools is advantageous
Experience within a pharmaceutical or CRO environment preferred
Technical & Professional Skills
Understanding of clinical quality systems and issue management frameworks
Experience performing root cause analysis and supporting CAPA implementation
Proficiency in data analysis tools such as Excel, Power BI, or other visualization platforms
Strong written and verbal communication skills in English
Ability to work effectively in a global matrix environment
High attention to detail with structured documentation practices
Working Model
This is a hybrid role requiring regular on-site presence in the local R&D office and collaboration with international teams.
Compensation (Poland Market Transparency)
For candidates hired in Poland, the annual base salary range is PLN 168,000 to PLN 280,000 gross, based on experience, qualifications, and market benchmarks. Additional bonus eligibility and performance-based awards may apply. Statutory and company-sponsored benefits are provided in accordance with local regulations.
Compensation for other locations will be discussed during the recruitment process in line with applicable market practices and transparency regulations.
Benefits & Career Growth
Hybrid working model (2–3 days per week in office)
Flexible working hours
Medical insurance and life coverage
Retirement and pension programs
Annual performance bonus eligibility
Professional development within a global biopharma organization
Exposure to global regulatory standards and governance frameworks
About GSK
GSK is a global biopharmaceutical company focused on uniting science, technology, and talent to get ahead of disease together. The organization develops innovative specialty medicines and vaccines across key therapeutic areas including respiratory, immunology, oncology, HIV, and infectious diseases.
With a strong commitment to patient safety, regulatory excellence, and scientific innovation, GSK provides professionals the opportunity to contribute meaningfully to global healthcare outcomes.
Equal Opportunity & Agency Notice
GSK is an Equal Opportunity Employer and evaluates qualified applicants without regard to protected characteristics under applicable laws.
GSK does not accept unsolicited agency referrals without prior written authorization from its procurement or human resources department.
This job listing is optimized for global search visibility in Clinical Compliance, Clinical Quality Assurance, Clinical Operations, GCP Monitoring, and Pharmaceutical Careers across Poland, India, and the United Kingdom on ThePharmaDaily.com.
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