Job Overview
Site: USA – Pennsylvania – Upper Providence, Belgium-Wavre, GSK HQ, UK – Hertfordshire – Stevenage, Warsaw
Posted: Apr 28 2026
Position Summary: Drive clinical compliance and continuous improvement within Development Operations. Work closely with clinical colleagues, quality partners, and global teams to monitor compliance, find root causes and deliver practical improvements. Help teams stay inspection ready while protecting patient safety and data integrity.
Responsibilities
- Build strong working relationships with Development Operations teams and stakeholders.
- Drive compliance with GCP, regulatory/legal requirements and GSK written standards.
- Ensure that issues and operational challenges are appropriately identified, managed, addressed and communicated within Development Operations teams.
- Collaborate closely with the R&D Quality & Risk Management organization to share information on potential risk areas and obtain insights into risks that require mitigation by Development Operations.
- Plan and execute Management Monitoring, targeted reviews, self‑assessments, data‑driven analysis and compliance monitoring.
- Ensure timely development, implementation and verification of corrective actions.
- Produce clear reports and governance materials for leadership and quality forums.
- Support audit and regulatory inspection preparation and responses as needed.
- Maintain business continuity planning and support activation when required.
Qualifications
- Bachelor’s degree in life sciences, clinical research, medicine, pharmacy, or related.
- At least 3 years of clinical operations experience supporting study delivery.
- Experience with ICH Good Clinical Practice (GCP) and applicable regulatory requirements.
- Experience with compliance monitoring, audits, or inspection preparation in clinical settings.
- Experience leading investigations and driving corrective and preventive actions to closure.
Preferred Qualifications
- Master’s degree in a relevant scientific or clinical field.
- Experience performing root cause analysis and integrating quality system approaches.
- Experience supporting regulatory inspections or audit responses.
- Ability to analyze operational metrics and convert them into practical improvements.
- Experience in the use of Artificial Intelligence for data analytics and monitoring.
- Familiarity with clinical systems and data visualization tools such as Veeva, Excel, and Power BI.
- Experience working in global or matrixed organizations and with external vendors or CROs.
- Strong written and verbal communication skills for clear reporting and stakeholder engagement.
Compensation
The annual base salary in Poland for new hires in this position ranges from PLN 261,000 to PLN 435,000 gross. The position may also be eligible for a bonus, awards for exceptional performance, and statutory benefits in accordance with Polish law. Other benefits may include private healthcare, additional paid days off, life insurance, private pension plan, and paid parental leave.
Equal Opportunity
GSK is an Equal Opportunity Employer. This ensures that all qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex (including pregnancy, gender identity, and sexual orientation), parental status, national origin, age, disability, genetic information, military service or any basis prohibited under federal, state or local law.
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