Find a job 
Featured Companies 
Featured Universities 
For Companies At a Glance
- Tasks: Support clinical compliance and improve operations while ensuring patient safety.
- Company: Join a leading global biopharma company dedicated to health innovation.
- Benefits: Flexible hybrid working, competitive salary, and extensive benefits package.
- Why this job: Make a real impact on clinical trials and patient safety in a collaborative environment.
- Qualifications: Degree in life sciences or related field; experience in clinical operations preferred.
- Other info: Dynamic team with strong learning opportunities and career progression.
The predicted salary is between 36000 - 60000 £ per year.
You will join the Clinical Compliance & Improvement (CCI) team to support clinical compliance, early issue detection and continuous improvement across Development Operations. You will work with colleagues in clinical teams, quality, and operations to gather data, perform compliance monitoring activities, and help deliver practical solutions. We value clear thinking, attention to detail, a collaborative mindset, and curiosity. This role offers strong learning and development, real influence on how trials are run, and the chance to help ensure patient safety and data integrity as we unite science, technology and talent to get ahead of disease together.
This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:
- Support compliance monitoring activities to detect trends, signals and emerging operational risks across assigned clinical teams.
- Help carry out compliance checks, management monitoring and follow-up activities to confirm corrective actions are effective.
- Collect, analyze and present compliance data and insights to inform improvement plans and priorities.
- Assist with issue governance activities including logging, tracking, escalation and communication of actions and outcomes.
- Support inspection and audit readiness activities by preparing documentation, responses and evidence as required.
- Contribute to continuous improvement projects, including data collection, root cause analysis and small project management tasks.
We are seeking professionals with the following required skills and qualifications to help us achieve our goals:
- Degree in a life science, pharmacy, nursing, clinical research or related discipline, or equivalent experience.
- 1–5 years' experience in clinical operations, quality, compliance, or a related function.
- Practical knowledge of Good Clinical Practice (GCP) and clinical trial conduct.
- Experience working with data to identify trends, signals or process gaps.
- Good written and verbal communication skills in English.
- Able to work in a hybrid model with regular time in the local R&D office.
If you have the following characteristics, it would be a plus:
- Experience supporting regulatory inspections or internal audits.
- Familiarity with clinical quality systems, issue management tools, or study oversight processes.
- Experience with root cause analysis and implementing corrective and preventive actions.
- Comfort working across multiple teams and stakeholders in a matrix environment.
- Proficiency with data analysis tools (Excel, Power BI, Artificial Intelligence, visualization tools), and clear reporting skills.
- Familiarity with clinical systems such as Veeva.
- Prior experience in a pharmaceutical or contract research environment.
What you will bring:
- Attention to detail and a disciplined approach to documentation and follow-up.
- A problem-solving mindset that looks for practical and sustainable solutions.
- Strong interpersonal skills to build working relationships across clinical, quality and operational partners.
- Integrity and a focus on patient safety and data integrity.
- Willingness to learn, adapt and take on new responsibilities to grow your career.
What we offer:
- Performance with Choice – flexibility in working mode (hybrid working model 2/3 days per week in the office), flexible working hours.
- Established job in an international, well-known pharmaceutical company.
- Opportunity to work in professional team plays crucial role in maintaining GSK portfolio on the markets.
- Opportunity to work within GSK standards and documentation applied globally.
- Wide range of benefits (Medical Plan, Life Insurance, Employee Retirement Program, Sport and recreation cards, Recreation allowance, annual bonus).
- Supportive & friendly working environment.
We are looking for someone who thrives in a collaborative environment, is passionate about delivering results, and is eager to make a difference. If this sounds like you, we’d love to hear from you.
Clinical Compliance in Stevenage employer: Gsk
Contact Detail:
Gsk Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Compliance in Stevenage
✨Tip Number 1
Network like a pro! Reach out to your connections in the clinical field, attend industry events, and join relevant online groups. 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 researching the company and its culture. Understand their values and how they align with your own. This will help you answer questions more confidently and show that you're genuinely interested in being part of their team.
✨Tip Number 3
Practice your responses to common interview questions, especially those related to compliance and quality assurance. Use the STAR method (Situation, Task, Action, Result) to structure your answers and highlight your relevant experience.
✨Tip Number 4
Don’t forget to follow up after your interview! A simple thank-you email can go a long way in leaving a positive impression. Plus, it shows your enthusiasm for the role and keeps you on their radar.
We think you need these skills to ace Clinical Compliance in Stevenage
Some tips for your application 🫡
Tailor Your Application: Make sure to customise your CV and cover letter for the Clinical Compliance role. Highlight your relevant experience in clinical operations, quality, and compliance, and show us how your skills align with what we're looking for.
Showcase Your Attention to Detail: Since this role requires a disciplined approach to documentation, be sure to demonstrate your attention to detail in your application. Use clear formatting and check for any typos or errors before hitting send!
Be Clear and Concise: When writing your cover letter, keep it straightforward and to the point. We appreciate clarity, so make sure you communicate your key achievements and how they relate to the responsibilities of the role without rambling on.
Apply Through Our Website: We encourage you to apply directly through our website. This way, you can ensure your application reaches us quickly and efficiently, and you'll have access to all the latest updates about the role and our company.
How to prepare for a job interview at Gsk
✨Know Your Stuff
Make sure you brush up on Good Clinical Practice (GCP) and clinical trial conduct. Familiarise yourself with the specific compliance monitoring activities mentioned in the job description, as this will show your genuine interest and understanding of the role.
✨Data is Key
Since the role involves collecting and analysing compliance data, be prepared to discuss your experience with data analysis tools like Excel or Power BI. Bring examples of how you've used data to identify trends or solve problems in previous roles.
✨Show Your Collaborative Spirit
This position requires working across multiple teams, so highlight your interpersonal skills. Share examples of how you've successfully collaborated with others in a matrix environment, and demonstrate your ability to build strong working relationships.
✨Ask Smart Questions
Prepare thoughtful questions about the company's approach to clinical compliance and continuous improvement. This not only shows your curiosity but also your commitment to ensuring patient safety and data integrity, which are crucial for this role.