Find health data science Jobs in dublin, d

Experienced Clinical Research Associate - Ireland
IQVIA —Dublin, County Dublin
- Full-time
- No degree
- In-person
Principal Data Analyst
Optum —Dublin, County Dublin
- Full-time
- Microsoft Excel
- SQL
- Analysis skills
Analyst
Aon Corporation —Dublin, County Dublin
- Full-time
4d
Data Analyst
Holafly —Dublin, County Dublin
- Hybrid work
- SQL
- Analysis skills
- Bachelor's degree
- Annual leave
Chief Technology Officer
FOODHUB —Dublin, County Dublin
- €200,000–€400,000 a year
- Full-time
- Hospitality
- Computer Science
- In-person
- Annual leave
Quick apply
12h
Data Scientist
Allianz —Dublin, County Dublin
- Full-time
- Azure
- Computer Science
- Master's degree
12d
Releaser, QA
Baxter —Dublin, County Dublin
- No degree
- Communication skills
- Annual leave
5d
Principal Data Scientist
Optum —Dublin, County Dublin
- Full-time
- Computer Science
- Research
- Master's degree
Principal Clinical Data Science Lead
ICON Plc —Dublin, County Dublin
- Full-time
- Oracle
- Microsoft Office
- Project management
1d
Clinical Research Associate
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Bachelor's degree
- In-person
Patient Safety Partner
Roche —Dublin, County Dublin
- Nursing
- Master's degree
- Bachelor's degree
13d
Characterisation Scientist
National Institute for Bioprocessing Research and Training (NIBRT) —Dublin, County Dublin
- Doctoral degree
- English
- Annual leave
QC Analyst (Microbiology) - (12 Months Agency Contract)
Viatris —Baldoyle, County Dublin
- Full-time
- Microsoft Word
- Microsoft Excel
- Bachelor's degree
Data Scientist, GenAI
American International Group UK Limited, Ireland Branch & AIG Europe S.A. (Ireland Branch) —DUBLIN 1, County Dublin
- Full-time
- No degree
- Agile
- AI
Quick apply
2d
Senior Business Intelligence Analyst
Indeed —Dublin, County Dublin
- €63,000–€95,000 a year
- Full-time
- Doctoral degree
- Master's degree
- SQL
- Annual leave
Quick apply
14d
QC Analyst ( 6 Months Agency Contract )
Viatris —Baldoyle, County Dublin
- Full-time
- Microsoft Word
- Microsoft Excel
- Bachelor's degree
13d
Quality Engineer (NPI)
West Pharmaceutical Services —Dublin, County Dublin
- Engineering
- Manufacturing
- Communication skills
Project Manager, Laboratory
ICON Plc —Dublin, County Dublin
- Full-time
- Project management
- Bachelor's degree
- No degree
Data Management Officer
Concern Worldwide —Dublin, County Dublin
- €47,539–€52,821 a year
- Full-time
- Computer Science
- Data analysis skills
- SQL
12d
Clinical SDTM Programmer
ICON Plc —Dublin, County Dublin
- Full-time
- Computer Science
- Bachelor's degree
- No degree
1d

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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

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health data science jobs in dublin, d

Experienced Clinical Research Associate - Ireland

Principal Data Analyst

Analyst

Data Analyst

Chief Technology Officer

Data Scientist

Releaser, QA

Principal Data Scientist

Principal Clinical Data Science Lead

Clinical Research Associate

Patient Safety Partner

Characterisation Scientist

QC Analyst (Microbiology) - (12 Months Agency Contract)

Data Scientist, GenAI

Senior Business Intelligence Analyst

QC Analyst ( 6 Months Agency Contract )

Quality Engineer (NPI)

Project Manager, Laboratory

Data Management Officer

Clinical SDTM Programmer

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