Senior Director, Clinical Quality Assurance
About the role
This vacancy has now expired. Please click here to view live vacancies.
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. See all locations Learn more about Our Culture at ICON
Day in the life
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/07/2025
Summary
Precision at the Outset: The Strategic Role of Site Selection and Activation in Clinical Trials The success of any clinical trial begins well before the first patient is enrolled. Behind every sit
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/04/2025
Summary
Cybersecurity in Clinical Data Management In clinical research, data is both a vital asset and a significant responsibility. As trials become increasingly digitised and decentralised, the protectio
.png)
Teaser label
IndustryContent type
BlogsPublish date
07/03/2025
Summary
Finding the Specialisation for You Clinical research is a dynamic, multidisciplinary field that brings together scientific innovation, operational rigour and patient-centric thinking. While many
Similar jobs at ICON
Salary
Location
United States, Canada
Department
Clinical Trial Management
Location
Canada
United States
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
As a Senior Clinical Scientist you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Senior Clinical Scientist will support l
Reference
2025-120685
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa BennerSalary
Location
Mexico City
Department
Study Start Up
Location
Mexico City
Business Area
ICON Strategic Solutions
Job Categories
Study Start Up
Job Type
Permanent
Description
As a Study Support Assistant you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence
Reference
2025-120464
Expiry date
01/01/0001
Author
Rita VillavicencioAuthor
Rita VillavicencioSalary
Location
Canada
Department
Clinical Trial Management
Location
Canada
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
The Clinical Trial Liaison (CTL) role is designed to transform the clinical research site experience by making the customer experience a priority. This strategic role serves as a critical interface be
Reference
2025-120769
Expiry date
01/01/0001
Author
Kala MurphyAuthor
Kala MurphySalary
Location
United States
Department
Clinical Trial Management
Location
United States
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Trial Management
Job Type
Permanent
Description
The Clinical Trial Liaison (CTL) role is designed to transform the clinical research site experience by making the customer experience a priority. This strategic role serves as a critical interface be
Reference
2025-120768
Expiry date
01/01/0001
Author
Kala MurphyAuthor
Kala MurphySalary
Location
United States
Department
Regulatory, Drug Safety/ Quality Assurance & Other roles
Location
United States
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Other
Job Type
Permanent
Description
As a Sr. TAT (Targeted Alpha Therapeurics) Expert you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-120518
Expiry date
01/01/0001
Author
Melissa BennerAuthor
Melissa BennerSalary
Location
Chicago
Department
Clinical Monitoring
Location
Chicago
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Clinical Monitoring
Job Type
Permanent
Description
As a Clinical Research Associate you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence.
Reference
2025-119487
Expiry date
01/01/0001
Author
Monica HawkinsAuthor
Monica Hawkins