At a Glance
- Tasks: Guide clinical trial teams in navigating complex compliance challenges and ensure high-quality standards.
- Company: Join Novartis, a leader in healthcare innovation with a commitment to quality.
- Benefits: Flexible hybrid working, competitive salary, and opportunities for professional growth.
- Other info: Dynamic role with opportunities to influence outcomes in a fast-paced environment.
- Why this job: Make a real impact in clinical trials while collaborating with diverse teams globally.
- Qualifications: Advanced degree in science or engineering and experience in clinical operations.
The predicted salary is between 29970 - 36483 £ per year.
For Hybrid working, there is an expectation of 12 days per month onsite. This role can also be provided on a Remote working basis, subject to eligibility criteria. Eligibility for remote work can be discussed at the interview stage.
Location: Westworks, London, UK. Other Locations: Dublin, Ireland. Please apply to the Dublin advertisement for this location. Novartis is unable to offer relocation support: please only apply if accessible. Novartis is unable to sponsor Visas for this location.
Step into a role where your expertise helps Clinical Trial Teams navigate some of their most complex and high-risk decisions. As a GCP Compliance Manager – Clinical Programs & Trials, you will operate as a trusted partner embedded within the clinical trial environment, working across a portfolio of studies to provide expert guidance on Good Clinical Practice and support teams staying in compliance. You will support teams in solving complex scenarios which require careful risk-assessment — translating technical requirements into clear, actionable insights that enable informed decision-making.
Acting as a key point of contact across study leaders, vendor managers, and cross-functional stakeholders, you will enable issue resolution, strengthen inspection readiness, and ensure trials are delivered to the highest standards of quality and compliance. This is a role for a curious, solutions-oriented professional who thrives on investigation, collaboration, and influencing outcomes in a fast-paced, global clinical landscape.
Key Responsibilities- Provide compliance oversight for clinical programs and trials, ensuring adherence to Good Clinical Practice standards.
- Act as primary compliance partner to Clinical Trial Teams, enabling decision-making on complex regulatory scenarios.
- Lead cross-functional discussions and resolution of quality issues using structured investigation and root cause analysis.
- Translate complex regulatory requirements into clear, actionable guidance for cross-functional clinical stakeholders.
- Coordinate inspection readiness activities, including preparation and inspection management, in addition to subsequent CAPA management.
- Monitor key indicators and trends to detect early signals of portfolio issues and support proactive mitigation strategies.
- Deliver self-assessment checks and controls, sharing insights to strengthen compliance and continuous improvement.
- Collaborate across functions, including Quality Assurance and Development, to ensure aligned and effective compliance practices.
- Support quality assessments of programs and trials and enable informed, risk-based decision-making.
- Champion a strong culture of quality, data integrity, and accountability across Global Clinical Operations and beyond.
- Advanced degree in science, engineering, or related discipline.
- Significant experience in clinical operations and clinical trial management within a pharmaceutical or healthcare environment.
- Strong knowledge of Good Clinical Practice standards and global regulatory requirements.
- Proven ability to investigate complex issues, perform root cause analysis, and develop effective corrective actions.
- Excellent communication skills with the ability to translate technical compliance concepts into clear, practical guidance.
- Strong problem-solving mindset with curiosity and ability to navigate ambiguity and regulatory trade-offs.
- Demonstrated ability to work effectively in cross-functional, matrixed teams and influence diverse stakeholders.
- Ability to work independently, manage multiple trials simultaneously, and prioritise across competing demands.
- Experience supporting audits and inspections, including preparation and interaction with health authority inspections.
- Openness to adopting and experimenting with artificial intelligence and new technologies to optimize ways of working.
GCP Compliance Manager - Clinical Programs & Trials in London employer: Novartis
At Novartis, we pride ourselves on being an exceptional employer, offering a dynamic work culture that fosters collaboration and innovation in the heart of London. Our GCP Compliance Manager role not only provides competitive benefits and opportunities for professional growth but also allows you to make a meaningful impact in clinical trials, ensuring the highest standards of quality and compliance. Join us to be part of a team that values your expertise and supports your career development in a fast-paced, global environment.
StudySmarter Expert Advice🤫
We think this is how you could land GCP Compliance Manager - Clinical Programs & Trials in London
✨Network Like a Pro
Get out there and connect with people in the industry! Attend events, join online forums, or even reach out on LinkedIn. We all know that sometimes it’s not just what you know, but who you know that can help you land that GCP Compliance Manager role.
✨Ace the Informational Interview
Don’t be shy about asking for informational interviews with professionals in clinical operations. This is your chance to learn more about the field and make a great impression. Plus, it shows your genuine interest in the role and the company!
✨Showcase Your Problem-Solving Skills
During interviews, be ready to share examples of how you've tackled complex issues in the past. We want to hear about your thought process and how you navigated ambiguity. This will demonstrate your fit for the fast-paced environment of clinical trials.
✨Apply Through Our Website
Make sure 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 serious about joining our team at Novartis.
We think you need these skills to ace GCP Compliance Manager - Clinical Programs & Trials in London
Some tips for your application 🫡
Tailor Your CV:Make sure your CV is tailored to the GCP Compliance Manager role. Highlight your experience in clinical operations and compliance, and don’t forget to sprinkle in those keywords from the job description. We want to see how your background aligns with what we’re looking for!
Craft a Compelling Cover Letter:Your cover letter is your chance to shine! Use it to tell us why you’re passionate about clinical trials and compliance. Share specific examples of how you've tackled complex regulatory scenarios in the past. We love a good story that showcases your problem-solving skills!
Showcase Your Communication Skills:Since this role involves working with various stakeholders, make sure to highlight your communication skills. Whether it’s through your CV or cover letter, demonstrate how you’ve effectively translated complex concepts into clear guidance for teams. We’re all about clarity and collaboration!
Apply Through Our Website:Don’t forget to apply through our website! It’s the best way for us to receive your application and ensures you’re considered for the role. Plus, it gives you a chance to explore more about StudySmarter and what we stand for. We can’t wait to hear from you!
How to prepare for a job interview at Novartis
✨Know Your GCP Inside Out
Make sure you brush up on Good Clinical Practice (GCP) standards before the interview. Be ready to discuss how you've applied these principles in past roles, especially in complex scenarios. This will show that you’re not just familiar with the regulations but can also translate them into actionable insights.
✨Showcase Your Problem-Solving Skills
Prepare examples of how you've tackled challenging compliance issues in previous positions. Use the STAR method (Situation, Task, Action, Result) to structure your responses. This will help demonstrate your analytical mindset and ability to navigate ambiguity effectively.
✨Communicate Clearly and Confidently
Since this role involves liaising with various stakeholders, practice articulating complex regulatory concepts in simple terms. You might even want to do a mock interview with a friend to refine your communication skills. Clear communication is key to influencing outcomes!
✨Be Ready for Scenario-Based Questions
Expect questions that put you in hypothetical situations related to compliance oversight or inspection readiness. Think about how you would approach these scenarios and be prepared to discuss your thought process. This will highlight your critical thinking and decision-making abilities.
