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For Companies At a Glance
- Tasks: Lead cross-functional teams to enhance clinical quality and compliance.
- Company: Join ICON plc, a leader in healthcare intelligence and clinical research.
- Benefits: Competitive salary, health insurance, flexible benefits, and global support programmes.
- Why this job: Make a real impact on clinical development and improve patient outcomes.
- Qualifications: Experience in clinical trials and managing Quality Events is essential.
- Other info: Inclusive culture with opportunities for personal and professional growth.
The predicted salary is between 36000 - 60000 £ per year.
ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.
The role is 100% embedded within a company that creates transformative medicines for people with serious diseases with a focus on specialty markets. You will play a key role in making improvements to how teams perform their work, supporting positive gains on compliance and reducing procedural complexity within the Clinical Quality Assurance team.
What You Will Be Doing
- Lead cross-functional teams to drive investigation, root cause analysis (RCA) and CAPA development for Global Clinical Operations (GCO) Quality Events (QEs).
- Author investigation summary, RCA, Impact Assessments and CAPA utilizing Veeva QMS.
- Ensure visibility to and manage awareness of any noted deviations, issues or deficiencies by escalating to management.
- Perform effectiveness checks, as assigned.
- Own and facilitate GCO planned deviations.
- Identifies and solves complex technical and operational problems, leveraging the appropriate resources.
- Liaise with Vertex clinical functions and external parties including CROs and Vendors to promote high level of quality and consistency across and within programs.
Your Profile
- A bachelor’s degree or master’s degree.
- Strong end to end clinical trial execution experience.
- Must have experience in managing Quality Events directly.
- Strong verbal/written communication, presentation and interpersonal skills.
- Familiarity with Veeva QMS system.
- In-depth understanding of GCP, ICH guidelines, CFR and ROW equivalents.
- Excellent verbal and written communication skills and presentation skills: ability to interact well with various team members and provide value added support to project.
- Demonstrated attention to detail, accuracy, excellent review and analytical skills in a fast-paced environment.
- Experience managing clinical quality activities and in-depth knowledge of clinical operations.
What ICON Can Offer You
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent. In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our Benefits Examples Include
- Various annual leave entitlements.
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized professionals who are there to support you and your family’s well-being.
- Life assurance.
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, among others.
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status.
If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know or submit a request here.
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
Senior GCP QA Manager in London employer: ICON Strategic Solutions
Contact Detail:
ICON Strategic Solutions Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Senior GCP QA Manager in London
✨Tip Number 1
Network like a pro! Reach out to your connections in the industry, especially those who work at ICON or similar companies. A friendly chat can open doors and give you insider info on the role.
✨Tip Number 2
Prepare for the interview by diving deep into GCP and ICH guidelines. Brush up on your knowledge of Veeva QMS too. We want you to shine when discussing how you can improve compliance and reduce complexity!
✨Tip Number 3
Showcase your problem-solving skills! Be ready to share examples of how you've tackled complex issues in past roles. This will demonstrate your ability to lead cross-functional teams effectively.
✨Tip Number 4
Don’t forget to apply through our website! It’s the best way to ensure your application gets the attention it deserves. Plus, we love seeing candidates who are proactive about their job search.
We think you need these skills to ace Senior GCP QA Manager in London
Some tips for your application 🫡
Tailor Your CV: Make sure your CV is tailored to the Senior GCP QA Manager role. Highlight your experience in managing Quality Events and your familiarity with GCP and ICH guidelines. We want to see how your skills align with what we’re looking for!
Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical research and how your background makes you a great fit for our team. We love seeing genuine enthusiasm!
Showcase Your Communication Skills: Since strong verbal and written communication skills are key for this role, make sure your application reflects that. Keep your language clear and professional, and don’t forget to proofread for any typos!
Apply Through Our Website: We encourage you to apply directly through our careers site. It’s the best way to ensure your application gets into the right hands. Plus, you can explore more about what we offer at ICON while you’re there!
How to prepare for a job interview at ICON Strategic Solutions
✨Know Your GCP Inside Out
Make sure you brush up on your Good Clinical Practice (GCP) knowledge. Be ready to discuss how you've applied GCP guidelines in your previous roles, especially in managing Quality Events. This will show that you understand the importance of compliance and can contribute to maintaining high standards.
✨Showcase Your Problem-Solving Skills
Prepare examples of complex technical or operational problems you've solved in past roles. Use the STAR method (Situation, Task, Action, Result) to structure your answers. This will demonstrate your analytical skills and ability to lead cross-functional teams effectively.
✨Familiarise Yourself with Veeva QMS
Since familiarity with Veeva QMS is a requirement, make sure you know its functionalities and how it supports quality management processes. If you have specific experiences using Veeva, be ready to share them during the interview to highlight your hands-on expertise.
✨Communicate Clearly and Confidently
Strong verbal and written communication skills are crucial for this role. Practice articulating your thoughts clearly and confidently. Consider doing mock interviews with a friend or using online resources to refine your presentation skills, ensuring you can engage effectively with various team members.
