Senior GCP QA Manager

Senior GCP QA Manager

Full-Time 36000 - 60000 £ / year (est.) No home office possible
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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 in clinical development and improve patient outcomes.
  • 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 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 employer: ICON Strategic Solutions

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 a strong focus on work-life balance, alongside numerous opportunities for professional growth within the world's largest clinical research organisation. With a commitment to diversity and employee well-being, ICON fosters a culture where your contributions are valued and rewarded, making it an ideal place for those seeking meaningful and impactful careers.
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Contact Detail:

ICON Strategic Solutions 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! Create a portfolio or a presentation that highlights your experience with Quality Events and CAPA development. This can set you apart during interviews and demonstrate your hands-on knowledge.

✨Tip Number 4

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

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

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

Some tips for your application 🫡

Tailor Your CV: Make sure your CV reflects the skills and experiences that match the Senior GCP QA Manager role. Highlight your clinical trial execution experience and any relevant quality management activities to catch our eye!

Craft a Compelling Cover Letter: Use your cover letter to tell us why you're passionate about clinical research and how your background aligns with our mission at ICON. A personal touch can really make you stand out from the crowd!

Showcase Your Communication Skills: Since strong verbal and written communication is key for this role, ensure your application materials are clear, concise, and free of errors. This is your chance to demonstrate your attention to detail!

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 and shows us you’re serious about joining our team!

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. Understand the latest ICH guidelines and CFR regulations, as these will likely come up during your interview. Being able to discuss how you've applied these principles in past roles will show you're not just familiar with them, but that you can leverage them effectively.

✨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 responses. This will demonstrate your analytical skills and ability to drive improvements within clinical operations, which is crucial for the Senior GCP QA Manager role.

✨Familiarise Yourself with Veeva QMS

Since the role involves using Veeva QMS, it’s a good idea to get comfortable with this system if you haven't already. If you have experience with it, be ready to discuss specific instances where you’ve used it to manage Quality Events or CAPA development. This will show that you’re prepared to hit the ground running.

✨Communicate Effectively

Strong verbal and written communication skills are essential for this position. Practice articulating your thoughts clearly and concisely. You might even want to prepare a short presentation on a relevant topic to showcase your presentation skills. This will help you stand out and demonstrate your ability to interact well with various team members.

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