Senior GCP QA Manager
Senior GCP QA Manager

Senior GCP QA Manager

Full-Time 43200 - 72000 £ / year (est.) No home office possible
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At a Glance

  • Tasks: Lead teams to improve clinical quality and manage compliance in a dynamic environment.
  • Company: Join ICON plc, a leader in healthcare intelligence and clinical research.
  • Benefits: Competitive salary, health insurance, flexible benefits, and work-life balance.
  • Why this job: Make a real impact on clinical development and transform lives through innovative medicines.
  • Qualifications: Experience in clinical trials, quality management, and strong communication skills.
  • Other info: Inclusive culture with opportunities for personal and professional growth.

The predicted salary is between 43200 - 72000 £ 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.

As a Senior GCP QA Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. 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 employer: ICON

ICON plc is an exceptional employer, offering a dynamic and inclusive work environment that prioritises innovation and excellence in the healthcare sector. As a Senior GCP QA Manager, you will benefit from competitive salaries, comprehensive health insurance, and flexible benefits tailored to support your well-being and work-life balance. With a strong focus on employee growth and development, ICON fosters a culture that rewards high performance and encourages collaboration across diverse teams, making it an ideal place for those seeking meaningful and impactful careers in clinical research.
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Contact Detail:

ICON Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Senior GCP QA Manager

✨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 lead to insider info about job openings and even referrals.

✨Tip Number 2

Prepare for interviews by practising common questions related to GCP and clinical quality assurance. We recommend doing mock interviews with friends or using online platforms to boost your confidence and refine your answers.

✨Tip Number 3

Showcase your expertise! Bring along examples of your past work, especially any CAPA development or RCA you've led. This will help you stand out and demonstrate your hands-on experience during interviews.

✨Tip Number 4

Don’t forget to apply through our website! It’s the best way to ensure your application gets seen by the right people. Plus, it shows you’re genuinely interested in joining the ICON team.

We think you need these skills to ace Senior GCP QA Manager

GCP (Good Clinical Practice)
ICH Guidelines
CFR (Code of Federal Regulations)
Veeva QMS
Root Cause Analysis (RCA)
CAPA (Corrective and Preventive Action)
Clinical Trial Execution
Quality Event Management
Analytical Skills
Communication Skills
Interpersonal Skills
Attention to Detail
Problem-Solving Skills
Project Management
Clinical Operations Knowledge

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Senior GCP QA Manager role. Highlight your relevant experience in clinical trial execution and quality management, and don’t forget to mention your familiarity with Veeva QMS!

Craft a Compelling Cover Letter: Your cover letter is your chance to shine! Use it to explain why you’re passionate about clinical quality assurance and how your skills align with our mission at ICON. Keep it concise but impactful!

Showcase Your Communication Skills: Since strong verbal and written communication skills are key for this role, make sure your application reflects that. Use clear language and structure your documents well to demonstrate your attention to detail.

Apply Through Our Website: We encourage you to apply through our careers site. It’s the best way to ensure your application gets seen by the right people. Plus, you’ll find more info about the benefits we offer!

How to prepare for a job interview at ICON

✨Know Your GCP Inside Out

Make sure you brush up on your Good Clinical Practice (GCP) knowledge. Understand the latest ICH guidelines and CFR regulations, as well as how they apply to clinical trial execution. Being able to discuss these in detail will show that you're not just familiar with the concepts but can also apply them practically.

✨Showcase Your Problem-Solving Skills

Prepare examples of complex technical and operational problems you've solved in previous roles. Use the STAR method (Situation, Task, Action, Result) to structure your answers. This will demonstrate your analytical skills and ability to drive improvements in compliance and procedural complexity.

✨Familiarise Yourself with Veeva QMS

Since the role involves using Veeva QMS for CAPA development and RCA, make sure you have a solid understanding of this system. If possible, get hands-on experience or review case studies that highlight its application in clinical quality assurance.

✨Communicate Effectively

Practice your verbal and written communication skills. Be ready to present your ideas clearly and concisely, especially when discussing investigation summaries or impact assessments. Remember, strong interpersonal skills are key in liaising with cross-functional teams and external parties.

Senior GCP QA Manager
ICON
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  • Senior GCP QA Manager

    Full-Time
    43200 - 72000 £ / year (est.)
  • I

    ICON

    10000+
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