At a Glance
- Tasks: Drive clinical compliance and improve processes in a dynamic 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: Opportunity for career growth and development in a supportive team.
- Why this job: Make a real impact on patient safety and data integrity while collaborating globally.
- Qualifications: Bachelor’s degree in life sciences and 3 years of clinical operations experience required.
The predicted salary is between 46100 - 76900 £ per year.
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 Stevenage employer: Gsk
Contact Detail:
Gsk Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Compliance and Improvement Manager in Stevenage
✨Network Like a Pro
Get out there and connect with folks in the clinical compliance world! Attend industry events, join relevant online forums, and don’t be shy about reaching out to people on LinkedIn. Building relationships can open doors that you didn’t even know existed.
✨Show Off Your Skills
When you get the chance to chat with potential employers, make sure to highlight your experience with GCP and compliance monitoring. Share specific examples of how you've driven improvements in past roles. We want to see your passion for patient safety and data integrity shine through!
✨Prepare for the Interview
Do your homework before any interview. Understand the company’s values and recent projects, especially in clinical operations. Prepare questions that show you’re genuinely interested in their work and how you can contribute to their goals. It’s all about making a great impression!
✨Apply Through Our Website
Don’t forget to apply directly through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re proactive and really keen on joining our team. Let’s get you that dream job!
We think you need these skills to ace Clinical Compliance and Improvement Manager in Stevenage
Some tips for your application 🫡
Know the Role: Before you start writing, make sure you really understand what the Clinical Compliance and Improvement Manager role is all about. Dive into the job description and highlight key responsibilities and qualifications that resonate with your experience.
Tailor Your Application: Don’t just send a generic CV and cover letter! We want to see how your skills and experiences align with the specific requirements of the role. Use keywords from the job description to show us you’re the perfect fit.
Showcase Your Achievements: When detailing your experience, focus on your achievements rather than just listing duties. Use numbers and examples to illustrate how you've driven compliance and improvements in past roles. We love seeing tangible results!
Keep It Professional Yet Personal: While we appreciate professionalism, don’t be afraid to let your personality shine through. A touch of authenticity can make your application stand out. And remember, apply through our website for the best chance!
How to prepare for a job interview at Gsk
✨Know Your Compliance Basics
Make sure you brush up on Good Clinical Practice (GCP) and relevant regulatory requirements. Being able to discuss these confidently will show that you understand the core of the role and can drive compliance effectively.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've identified issues in clinical operations and implemented corrective actions. Use the STAR method (Situation, Task, Action, Result) to structure your responses and highlight your analytical skills.
✨Build Relationships in Your Answers
Since this role involves collaboration with various teams, be ready to talk about how you've built strong working relationships in the past. Share specific instances where teamwork led to successful outcomes, especially in compliance or quality settings.
✨Be Data-Driven
Familiarise yourself with data analytics tools like Excel or Power BI. Be prepared to discuss how you've used data to drive improvements in previous roles. This will demonstrate your ability to analyse operational metrics and make informed decisions.