Senior Director, Clinical Quality Assurance
About the role
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Senior Director, Clinical Quality Assurance
Location: Leopardstown, Dublin 18
At ICON, it's our people that set us apart.
As a global provider of drug development solutions, our work is serious business. But that doesn't mean you can't have fun while you do it. With our vision to be the partner of choice in drug development, we hire only the best and brightest in the industry!
Are you one of them?
At ICON, we have an incredible opportunity for an expert Senior Director of Clinical Quality Assurance to join the team in our global HQ in Dublin 18.
The Role
Reporting to the VP of Quality Assurance, you will be responsible for leading and developing the Quality Assurance team ensuring that an effective structure is in place. Working collaboratively with other QA team across the business to ensure consistent quality standards are delivered. Partnering closely with ICON's clients to ensure first class support.
This role will involve travel up to 35%.
- Build and maintain an effective Quality Assurance function within the region.
- Lead, develop, grow and manage the Quality Assurance team, ensuring that an effective management structure is in place in the QA Team.
- Ensure that an effective audit program is implemented, in order to provide assurances that clinical studies managed by ICON are of the highest standard and are in compliance with the requirements of ICON or Sponsor SOPs, study protocols, relevant regulations and guidelines and with ISO 9000 requirements.
- Provide expertise and leadership in Quality Compliance to the wider organization, and ensure that all personnel are aware of the ICON requirements for quality.
- Proactively ensure that the ICON QMS procedures are updated in line with changes in laws, standards and regulations and to ensure process improvements, and meet business needs.
- Provides input/support to operational teams on issue resolution and process improvements.
- Serves as the division expert on Quality related matters.
- Provide ongoing feedback to senior management of quality compliance (metrics)
- Work closely with the QA teams in other regions to ensure consistent quality standards and to foster strong working relationships
- In conjunction with the Finance department, prepare the QA department budget and ensure effective cost control.
- Ensure that Sponsor and Regulatory audits are effectively executed and provide support and direction during the hosting of such audits as necessary.
- Participate in professional development through journal articles and by presenting at and attending conferences and professional meetings.
- Contribute to the growth of ICON by participating in stand-alone QA services, in collaboration with the business development group, and in line with market opportunities and available resources.
- Keep the person to whom the Senior Director reports informed of any quality issues within the department/office which require attention.
What you need
- A Degree within Life Sciences.
- A deep understanding of clinical trials and processes involved.
- An experienced people leader who is always looking to develop and support their team in their careers at ICON.
- GCP regulatory experience is a necessity for this role as is an Audit background.
- A strategic thinker who sees critical issues that need to be acted upon.
- Forward thinking with the ability to see opportunities to improve the QA function.
- Excellent team member who has the ability to cultivate genuine relationships with our clients.
Why join us?
Other than working with an outstanding team of ambitious people, we also offer a very competitive benefits package. This varies from country to country so a dedicated recruiter will discuss this with you at interview stage.
We care about our people as they are the key to our success. We provide an open and friendly work environment where we empower people and provide them with opportunities to develop their long term career.
Ongoing development is vital to us, and as a Senior Director, Clinical Quality Assurance, you will have the opportunity to progress your career, with the potential to move into other related areas to improve your skillset. Our benefits package is competitive, our scope is international and we sincerely care about our people and their success.
ICON is an equal opportunity employer and committed to providing a workplace free of any discrimination or harassment.
EOE race/colour/religion/sex/sexual orientation/gender identity/disability/vet/national origin
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. Learn more about Our Culture at ICON
Day in the life
Teaser label
Our PeopleContent type
BlogsPublish date
12/10/2025
Summary
Zhong Yao's Journey at ICON Plc in China Zhong Yao's career in clinical research spans over two decades, with leadership roles across major CROs and a commitment to advancing healthcare in China.
Teaser label
IndustryContent type
BlogsPublish date
12/01/2025
Summary
How Data Moves Through a Clinical Trial Clinical research depends on one essential element: trustworthy data. Every safety decision, every statistical conclusion and every regulatory submission i
Teaser label
IndustryContent type
BlogsPublish date
11/28/2025
Summary
Quality and Compliance for New Entrants: A Plain Language Guide Quality and compliance can feel like dense subjects when you are entering clinical research for the first time. Many job
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