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- Tasks: Drive clinical compliance and improve processes in a dynamic healthcare environment.
- Company: Join GSK, a leading global healthcare company committed to innovation.
- Benefits: Competitive salary, private healthcare, extra paid days off, and a pension plan.
- Other info: Collaborative culture with opportunities for professional growth and development.
- Why this job: Make a real impact on patient safety and data integrity while advancing your career.
- Qualifications: Bachelor’s degree in life sciences and 3 years of clinical operations experience required.
The predicted salary is between 50000 - 80000 £ per year.
Site: USA - Pennsylvania - Upper Providence, Belgium-Wavre, GSK HQ, UK - Hertfordshire - Stevenage, Warsaw
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.
Clinical Compliance and Improvement Manager in London employer: Gsk
Contact Detail:
Gsk Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Compliance and Improvement Manager in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical field and let them know you're on the hunt for a Clinical Compliance and Improvement Manager role. You never know who might have the inside scoop on job openings or can put in a good word for you.
✨Tip Number 2
Prepare for interviews by brushing up on your knowledge of GCP and regulatory requirements. Be ready to discuss how you've tackled compliance challenges in the past. We want to see you shine, so practice articulating your experiences clearly and confidently!
✨Tip Number 3
Showcase your analytical skills! Be prepared to talk about how you've used data-driven analysis to improve processes in previous roles. Highlight any experience with tools like Veeva or Power BI, as this will set you apart from other candidates.
✨Tip Number 4
Don't forget to apply through our website! It’s the best way to ensure your application gets noticed. Plus, we love seeing candidates who are proactive and engaged with our company. So, get that application in and let’s make it happen!
We think you need these skills to ace Clinical Compliance and Improvement Manager in London
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Clinical Compliance and Improvement Manager role. Highlight your experience with GCP and compliance monitoring, as well as any relevant projects that showcase your ability to drive improvements.
Showcase Your Skills: Don’t forget to emphasise your strong written and verbal communication skills. We want to see how you can produce clear reports and engage stakeholders effectively, so include examples of your past work in this area.
Be Specific About Your Experience: When detailing your clinical operations experience, be specific about your roles and responsibilities. Mention any audits or inspections you've been involved in, and how you contributed to successful outcomes.
Apply Through Our Website: We encourage you to apply directly through our website. It’s the best way to ensure your application gets into the right hands and shows us you’re serious about joining our team!
How to prepare for a job interview at Gsk
✨Know Your Compliance Inside Out
Make sure you brush up on Good Clinical Practice (GCP) and any relevant regulatory requirements. Being able to discuss these confidently will show that you’re not just familiar with the rules, but that you can apply them in real-world scenarios.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've identified issues in clinical operations and driven corrective actions. Use the STAR method (Situation, Task, Action, Result) to structure your answers, making it easy for interviewers to see your impact.
✨Build Relationships Virtually
Since this role involves collaboration with various teams, think about how you can demonstrate your relationship-building skills. Share experiences where you’ve worked with cross-functional teams or external vendors to achieve compliance goals.
✨Be Data-Driven
Familiarise yourself with data analytics tools like Excel and Power BI. Be ready to discuss how you’ve used data to drive improvements in past roles. This will highlight your analytical skills and your ability to turn metrics into actionable insights.