JUMP TO CONTENT

Senior Director, Clinical Quality Assurance

JR062818

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

List #1

Day in the life

Headshot of male
25 Years in Clinical Operations at ICON: Ricardo Cortizo Justo Q&A

Teaser label

Our People

Content type

Blogs

Publish date

04/08/2026

Summary

Ricardo Cortizo Justo, Director of Clinical Operations and Site Head for Paris at ICON plc, recently marked an exceptional milestone of 25 years with the organisation. Over the course of his career, R

Teaser label

Ricardo shares insights from 25 years at ICON, covering clinical operations, leadership, and career development.

Read more
Heartbeat vitals on monitor
Central Monitoring vs On Site Monitoring

Teaser label

Industry

Content type

Blogs

Publish date

04/03/2026

Summary

Understanding Central Monitoring vs On Site Monitoring Monitoring is a core component of clinical trial oversight. It ensures that studies are conducted in line with the protocol, that data is re

Teaser label

Learn the difference between central monitoring and on site monitoring and how both support patient safety and data quality.

Read more
middle aged male wearing shirt
Francis' Journey back to ICON

Teaser label

Our People

Content type

Blogs

Publish date

03/26/2026

Summary

Why Francis returned to ICON: building a long-term career in clinical research Francis Kayamba is a Clinical Research Associate based in Johannesburg, South Africa. He first joined ICON in February

Teaser label

Francis Kayamba shares what drew him back to ICON and how the sponsor-embedded model works.

Read more
View all

Similar jobs at ICON

Clinical Research Associate

Salary

Location

China, Shanghai

Location

Shanghai

Remote Working

Remote or Office

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate (SSU) to join our diverse and dynamic team. As a Clinical Research Associate (SSU) at ICON, you will play a pivotal role in designing and analyzi

Reference

JR147871

Expiry date

01/01/0001

Jenny Zhang

Author

Jenny Zhang
Jenny Zhang

Author

Jenny Zhang
Read more Shortlist Save this role
Clinical Research Associate

Salary

Location

Brazil, Sao Paulo

Location

Sao Paulo

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

We are currently seeking a Clinical Research Associate in Belém do Pará to join our diverse and dynamic team. As a Clinical Research Associate at ICON, you will play a pivotal role in designing and an

Reference

JR138152

Expiry date

01/01/0001

Tulio Sanquiz

Author

Tulio Sanquiz
Read more Shortlist Save this role
Sr. CRA

Salary

Location

Atlanta,GA

Location

Atlanta

Texas

Maryland

Missouri

Tennessee

North Carolina

Illinois

Ohio

Florida

Philadelphia, PA

Remote Working

Remote

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 organization, powered by healthcare intelligence.What you will be doing:Implements and m

Reference

JR148386

Expiry date

01/01/0001

Monica Hawkins Read more Shortlist Save this role
Clinical Research Associate, Sponsor Dedicated

Salary

Location

US, Blue Bell (ICON)

Location

Blue Bell

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Monitoring

Job Type

Permanent

Description

As a CRA II 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

Reference

JR148554

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
Clinical Data Quality Associate

Salary

Location

Mexico, Mexico City

Department

Full Service - Early Clinical and Bioanalytical Solutions

Location

Mexico City

Remote Working

Hybrid

Business Area

ICON Full Service & Corporate Support

Job Categories

Clinical Data Management

Job Type

Permanent

Description

We are currently seeking a Clinical Data Quality Associate to join our diverse and dynamic team. As a Clinical Data Quality Associate at ICON, you will play a pivotal role in designing and analyzing c

Reference

JR146933

Expiry date

01/01/0001

Florencia  Borello Taiana Read more Shortlist Save this role
Clinical Trial Liaison, Sponsor Dedicated

Salary

Location

US, Raleigh, NC

Location

Raleigh

Remote Working

Remote

Business Area

ICON Strategic Solutions

Job Categories

Clinical Trial Liaison

Job Type

Permanent

Description

As a Clinical Trial Liaison 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 W

Reference

JR148515

Expiry date

01/01/0001

Jamie Pruitt

Author

Jamie Pruitt
Read more Shortlist Save this role
View Jobs

Browse popular job categories below or search all jobs above