Find clinical research associate Jobs in county dublin

Experienced Clinical Research Associate - Ireland
IQVIA —Dublin, County Dublin
- Full-time
- No degree
- In-person
Clinical Research Associate
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Bachelor's degree
- In-person
Clinical Trials Associate
Zymeworks Inc. —Swords, County Dublin
- €31,500–€48,300 a year
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Office
- Bachelor's degree
- Annual leave
Quick apply
6d
Clinical Quality Assurance - Program Lead (Associate Director)
Novartis —Dublin, County Dublin
- Full-time
- Doctoral degree
- Master's degree
- Bachelor's degree
Global Program Clinical Head (Neuroscience)
Novartis —Dublin, County Dublin
- Full-time
- Hybrid work
- Doctoral degree
- Communication skills
12d
Imaging Operations Manager, Clinical Studies
Novartis —Dublin, County Dublin
- Full-time
- English
- Business
- Leadership
PhD Researcher in Sociology
Trinity College Dublin —Dublin, County Dublin
- €25,000 a year
- Full-time
- Doctoral degree
- Teaching
Associate Director, Translational Medicine
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Doctoral degree
- Master's degree
- Project management
Basic grade Cardiac Physiologist Permanent
Tallaght University Hospital —Tallaght, County Dublin
- Master's degree
- Bachelor's degree
- No degree
- Annual leave
- Sick pay
4h
Vendor Alliance Lead Associate Director (Cardiac Safety and Respiratory Diagnostics)
Novartis —Dublin, County Dublin
- Full-time
- No degree
- Communication skills
5d
Principal Biostatistician (Biomarker Analyst -EMEA and US BASED)
サイネオス・ヘルス —Dublin, County Dublin
- English
- Communication skills
Principal Statistician Oncology with Submission Experience
サイネオス・ヘルス —Dublin, County Dublin
- Doctoral degree
- English
- Communication skills
2d
Senior Principal Clinical Data Scientist
Novartis —Dublin, County Dublin
- Full-time
- Master's degree
- Mentoring
- Organisational skills
Head of Data Governance, Anonymization and Quality
Novartis —Dublin, County Dublin
- Full-time
- Doctoral degree
- Computer Science
- Research
12d
Clinical Development Director - Renal
Novartis —Dublin, County Dublin
- Full-time
- Doctoral degree
- Writing skills
- No degree
13d
Associate Director, Statistical Programming
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Doctoral degree
- Computer Science
- Master's degree
Manager, Finished Goods Supply Planning ( Remote Ireland)
Beckman Coulter Diagnostics —Dublin, County Dublin
- Full-time
- Remote
- Master's degree
- Bachelor's degree
- Communication skills
- Annual leave
Associate Director, Biostatistics
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Doctoral degree
- English
- Master's degree
The Associate Director, Linux/Unix Admin
IQVIA —Dublin, County Dublin
- Full-time
- Azure
- Oracle
- Computer Science
Associate Biostatistics Director - FSP (Permanent Home-based)
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- Doctoral degree
- Leadership
- Communication skills

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Experienced Clinical Research Associate - Ireland

IQVIA -
Dublin, County Dublin

Apply Now

Job details

Full-time

Full job description

Dublin, Ireland | Full time | Field-based | R1539313

Join Us on Our Mission to Drive Healthcare Forward

IQVIA site management (full service) are seeking experienced Clinical Research Associates in the Republic of Ireland.

With access to world-class training and professional development, we’ll give you the tools you need to create the career you want.

Why IQVIA?

IQVIA is recognized as #1 in its category on the 2026 Fortune® World’s Most Admired Companies™ list for the fifth consecutive year!
We offer genuine career development opportunities for those who want to grow as part of the organization.
The chance to work on cutting edge medicines at the forefront of new medicines development.
IQVIA has access to significant data pools allowing better site selection and recruitment. This helps drive performance of sites making the CRA role more efficient and discussions at site more productive. Next generation clinical development!

Responsibilities

Perform site monitoring visits (selection, initiation, monitoring and close-out visits) in accordance with contracted scope of work and regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Work with sites to adapt, drive, and track subject recruitment plan in line with project needs to enhance predictability
Administer protocol and related study training to assigned sites and establish regular lines of communication with sites to manage ongoing project expectations and issues
Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations. Escalate quality issues as appropriate
Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution. May support start-up phase
Ensure copies/originals (as required) site documents are available for filing in the Trial Master File (TMF) and verify that the Investigator's Site File (ISF) is maintained in accordance with GCP and local regulatory requirements
Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans by submitting regular visit reports, generating follow-up letters and other required study documentation
Collaborate and liaise with study team members for project execution support as appropriate

Requirements

A minimum of 18 months of independent on-site monitoring
You have successfully managed multiple clinical trial protocols across diverse investigative sites.
In depth knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines
Life science degree educated or equivalent industry experience
Flexibility to travel to sites

Apply today and forge a career with greater purpose, make an impact, and never stop learning!

*Please note - this role is not eligible for UK visa sponsorship*

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

Apply Now

Refine Your Search

clinical research associate jobs in county dublin

Experienced Clinical Research Associate - Ireland

Clinical Research Associate

Clinical Trials Associate

Clinical Quality Assurance - Program Lead (Associate Director)

Global Program Clinical Head (Neuroscience)

Imaging Operations Manager, Clinical Studies

PhD Researcher in Sociology

Associate Director, Translational Medicine

Basic grade Cardiac Physiologist Permanent

Vendor Alliance Lead Associate Director (Cardiac Safety and Respiratory Diagnostics)

Principal Biostatistician (Biomarker Analyst -EMEA and US BASED)

Principal Statistician Oncology with Submission Experience

Senior Principal Clinical Data Scientist

Head of Data Governance, Anonymization and Quality

Clinical Development Director - Renal

Associate Director, Statistical Programming

Manager, Finished Goods Supply Planning ( Remote Ireland)

Associate Director, Biostatistics

The Associate Director, Linux/Unix Admin

Associate Biostatistics Director - FSP (Permanent Home-based)

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