Ccqm

Full-Time 60000 - 75000 £ / year (est.) Home office (partial)
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At a Glance

  • Tasks: Lead quality assurance in clinical trials and ensure compliance with industry standards.
  • Company: Join ICON, a leading healthcare intelligence and clinical research organisation.
  • Benefits: Enjoy competitive salary, health insurance, flexible benefits, and work-life balance.
  • Other info: Inclusive culture with opportunities for career growth and personal development.
  • Why this job: Make a real impact on innovative treatments while developing your leadership skills.
  • Qualifications: Bachelor's degree in a relevant field and experience in clinical quality assurance.

The predicted salary is between 60000 - 75000 £ 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 Clinical Quality Compliance Lead at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.

What You Will Do:

  • You will oversee quality assurance and compliance workstreams, ensuring deliverables meet quality and timeline expectations.
  • Develop and implement comprehensive quality management systems and processes to ensure compliance with regulatory requirements, industry standards, and company policies.
  • Lead internal and external audits and inspections, including planning, execution, and follow-up activities to address findings and ensure timely resolution.
  • Conduct regular quality reviews of clinical trial documentation, protocols, and study reports, identifying areas for improvement and implementing corrective actions as necessary.
  • Provide leadership and guidance to the clinical quality compliance team, including training, mentoring, and performance management.
  • Collaborate with cross-functional teams to assess quality risks, develop risk mitigation strategies, and drive continuous improvement initiatives.

Your Profile:

You will have solid quality assurance and compliance experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

  • Bachelor's degree or higher in a relevant scientific discipline or healthcare-related field.
  • Previous experience in clinical quality assurance or compliance within the pharmaceutical, biotechnology, or CRO industry.
  • Expert knowledge of regulatory requirements, including FDA/EMA regulations, ICH-GCP guidelines, and ISO standards.
  • Strong leadership and project management skills, with the ability to effectively prioritize tasks and manage resources to meet objectives.
  • Excellent communication, interpersonal, and problem-solving skills, with the ability to influence and collaborate with stakeholders at all levels of the organization.
  • Willingness to travel to site as required about once per month.

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, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised 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, subsidised 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.

Ccqm employer: IRE

At ICON plc, we pride ourselves on being a world-leading healthcare intelligence and clinical research organisation that champions innovation and excellence. Our inclusive work culture fosters collaboration and personal growth, offering competitive benefits such as comprehensive health insurance, flexible leave entitlements, and a global employee assistance programme. Join us in shaping the future of clinical development while enjoying a supportive environment that values your contributions and well-being.
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Contact Detail:

IRE Recruiting Team

StudySmarter Expert Advice 🤫

We think this is how you could land Ccqm

✨Tip Number 1

Network like a pro! Reach out to your connections in the industry, attend relevant events, and don’t be shy about asking for introductions. We all know that sometimes it’s not just what you know, but who you know that can help you land that dream job.

✨Tip Number 2

Prepare for interviews by researching ICON and understanding their values and mission. We want to see that you’re genuinely interested in the role and the company. Tailor your answers to reflect how your experience aligns with their goals, especially in quality compliance.

✨Tip Number 3

Practice makes perfect! Conduct mock interviews with friends or mentors to refine your responses. Focus on articulating your experience in quality assurance and compliance clearly, as this will showcase your expertise and confidence during the real deal.

✨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. We appreciate candidates who show enthusiasm and professionalism, so make sure to express your gratitude for the opportunity.

We think you need these skills to ace Ccqm

Quality Assurance
Compliance Management
Regulatory Knowledge
FDA/EMA Regulations
ICH-GCP Guidelines
ISO Standards
Leadership Skills
Project Management
Communication Skills
Interpersonal Skills
Problem-Solving Skills
Risk Assessment
Continuous Improvement
Training and Mentoring

Some tips for your application 🫡

Tailor Your CV: Make sure your CV is tailored to the Clinical Quality Compliance Lead role. Highlight your relevant experience in quality assurance and compliance, and don’t forget to mention any specific regulatory knowledge you have. 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 explain why you're passionate about clinical quality compliance and how your skills can contribute to our mission at ICON. Keep it concise but impactful – we love a good story!

Showcase Your Leadership Skills: Since this role involves leading a team, make sure to highlight your leadership experience. Share examples of how you've mentored or guided others in previous roles. We’re keen to see how you can inspire and develop our clinical quality compliance team!

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’ll find all the info you need about the role and our awesome benefits there!

How to prepare for a job interview at IRE

✨Know Your Regulations

Familiarise yourself with FDA/EMA regulations, ICH-GCP guidelines, and ISO standards. Being able to discuss these in detail will show your expertise and readiness for the role.

✨Showcase Your Leadership Skills

Prepare examples of how you've led teams or projects in the past. Highlight your experience in training and mentoring others, as this is crucial for the Clinical Quality Compliance Lead position.

✨Be Ready for Scenario Questions

Expect questions about how you would handle specific compliance issues or audit findings. Think through potential scenarios and your approach to resolving them effectively.

✨Demonstrate Cross-Functional Collaboration

Prepare to discuss how you've worked with different teams to assess quality risks and implement improvements. This will illustrate your ability to collaborate and drive initiatives across the organisation.

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