Find clinical data management Jobs in dublin county dublin

Experienced Clinical Research Associate - Ireland
IQVIA —Dublin, County Dublin
- Full-time
- No degree
- In-person
Clinical Terminologist
Optum —Dublin, County Dublin
- Full-time
- Data analysis skills
- AI
- Python
Clinical Data Management Lead, home-based
IQVIA —Dublin, County Dublin
- Full-time
- Remote
- Customer service
- Project management
- Bachelor's degree
Specialist Coordinator for Centre of Education
Beaumont Hospital —Dublin, County Dublin
- €73,062–€81,989 a year
- Research
- No degree
- Leadership
13d
Clinical Governance Administrator
Medica —Dublin, County Dublin
- Full-time
- Hybrid work
- Microsoft Excel
- Microsoft Outlook
- Administrative experience
Quick apply
4h
Principal Clinical Data Science Lead
ICON Plc —Dublin, County Dublin
- Full-time
- Oracle
- Microsoft Office
- Project management
1d
Research Assistant - Dementia Clinical Trials Coordinator
Trinity College Dublin —Dublin, County Dublin
- Full-time
- Clinic
5d
Pharma Partnerships Manager
Optum —Dublin, County Dublin
- Full-time
- Negotiation
Clinical SDTM Programmer
ICON Plc —Dublin, County Dublin
- Full-time
- Computer Science
- Bachelor's degree
- No degree
1d
Clinical Research Associate
Grifols Worldwide Op Ltd —Dublin, County Dublin
- Full-time
- Bachelor's degree
- In-person
Clinical Research Assistant
Trinity College Dublin (TCD) —Dublin, County Dublin
- €32,000–€36,272 a year
- Full-time
- English
- Master's degree
- Project management
Quick apply
6d
Investigator Payments Systems Analyst
ICON Plc —Dublin, County Dublin
- Full-time
- Bachelor's degree
- Budgeting
- Communication skills
2d
Patient Safety Partner
Roche —Dublin, County Dublin
- Nursing
- Master's degree
- Bachelor's degree
13d
Senior Scientific Writer II
Novartis —Dublin, County Dublin
- Full-time
- Doctoral degree
- English
- Bachelor's degree
Area Support Manager
IVC —Dublin, County Dublin
- Remote
- Communication skills
Health & Social Care Transformation Consultant, Hybrid
Deloitte —Dublin, County Dublin
- Full-time
- Hybrid work
GCP Compliance Manager - Clinical Programs & Trials
Novartis —Dublin, County Dublin
- Full-time
- Engineering
- Communication skills
1d
Data Migration Specialist
Lanas Healthcare Technology Ltd —DUBLIN 24, County Dublin
- Computer Science
- SQL
- Analysis skills
- Annual leave
- Employee assistance program
Quick apply
6d
Project Manager, Laboratory
ICON Plc —Dublin, County Dublin
- Full-time
- Project management
- Bachelor's degree
- No degree
Principal Clinical Data Scientist
Novartis —Dublin, County Dublin
- Full-time
- Master's degree
- Organisational skills
- Agile

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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 data management jobs in dublin county dublin

Experienced Clinical Research Associate - Ireland

Clinical Terminologist

Clinical Data Management Lead, home-based

Specialist Coordinator for Centre of Education

Clinical Governance Administrator

Principal Clinical Data Science Lead

Research Assistant - Dementia Clinical Trials Coordinator

Pharma Partnerships Manager

Clinical SDTM Programmer

Clinical Research Associate

Clinical Research Assistant

Investigator Payments Systems Analyst

Patient Safety Partner

Senior Scientific Writer II

Area Support Manager

Health & Social Care Transformation Consultant, Hybrid

GCP Compliance Manager - Clinical Programs & Trials

Data Migration Specialist

Project Manager, Laboratory

Principal Clinical Data Scientist

I want to receive the latest job alerts for clinical data management in dublin county dublin

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