Find pharmaceutical external Jobs in dublin, d

Clinical SDTM Programmer
ICON Plc —Dublin, County Dublin
- Full-time
- Computer Science
- Bachelor's degree
- No degree
3d
Pathology Project Manager
ICON Plc —Dublin, County Dublin
- Full-time
- Project management
- Bachelor's degree
- No degree
12d
Supervisor, Laboratory
ICON Plc —Dublin, County Dublin
- Overtime
- Master's degree
- Bachelor's degree
- No degree
- Annual leave
- Employee assistance program
Maintenance & Calibration Lead
Mallinckrodt —Dublin, County Dublin
- Full-time
- Manufacturing
- Leadership
- Communication skills
Global Supply Planner
AbbVie —Dublin, County Dublin
- Full-time
- Hybrid work
- Master's degree
- Analysis skills
- Bachelor's degree
Programme Director MSc in Procurement and Supply Chain Management
Griffith College —DUBLIN 8, County Dublin
- Full-time
- Management
- Doctoral degree
- Master's degree
- Free parking
- Work from home
Quick apply
8d
Senior Treasury Analyst
Takeda Pharmaceutical —Dublin, County Dublin
- €57,800–€79,420 a year
- Full-time
- Microsoft Excel
- Finance
- Business
Senior Manager - Network Supply Planning
Alexion Pharmaceuticals,Inc. —Dublin, County Dublin
- Microsoft Outlook
- Communication skills
Capital Sales Specialist - Life Science, Ireland
Getinge Ireland Ltd. —Dublin, County Dublin
- Sales
- English
- Analysis skills
19h
Senior Specialist Regulatory Key Initiatives
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Word
- Microsoft Excel
- Bachelor's degree
Tech Transfer Lead, Drug Substance
PSC Biotech —Dublin, County Dublin
- Full-time
- Doctoral degree
- Master's degree
- Project management
2d
Quality Engineering Manager
Embecta —Dún Laoghaire, County Dublin
- Full-time
- Engineering
- Communication skills
Associate, Contract Management
EVERSANA —Dublin, County Dublin
- Full-time
- Remote
- Management
- Salesforce
- Microsoft Office
Quick apply
CNC Machinist
Prodieco —Tallaght, County Dublin
- Evening shift
- Maths
- Mechanical knowledge
- Referral programme
Director Respiratory Regulatory CMC
Viatris —Northern Cross, County Dublin
- Full-time
- Microsoft Office
- Project management
- Manufacturing
Quality Manager, Global Distribution Quality
Amgen —Dublin, County Dublin
- Doctoral degree
- Master's degree
- Bachelor's degree
Senior Manager - Network Supply Planning
AstraZeneca —Dublin, County Dublin
- Microsoft Outlook
- Communication skills
Director of Network Pharmacy Contracting
Optum —Dublin, County Dublin
- Full-time
- Microsoft Powerpoint
- Sales
- Leadership
Geo-Environmental Consultant
AECOM —Dublin, County Dublin
- Full-time
- Hybrid work
- Engineering
- Bachelor's degree
- Communication skills
Treasury Manager/Senior Manager
Azurity Pharmaceuticals - Ireland —Dublin, County Dublin
- Communication skills
- Banking

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Clinical SDTM Programmer

ICON Plc -
Dublin, County Dublin

Apply Now

Job details

Full-time
3 days ago

Qualifications

Computer Science
XML
SAS
Data structures
Bachelor's degree
Communication skills

Full job description

Clinical SDTM Programmer (advanced)

ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.

As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.

We are recruiting an Advanced Clinical Programmer (SDTM) to support a long‑term FSP partnership with a global, top‑tier pharmaceutical company.

This role is highly focused on SDTM oversight, standards, and submission readiness, with direct visibility across study teams and regulatory deliverables.

About the Role

As an Advanced SDTM Clinical Programmer, you will provide end‑to‑end oversight of SDTM programming activities, from study set‑up through to submission‑ready packages. You will act as a technical authority on CDISC standards, ensuring quality, compliance, and consistency across trials while collaborating closely with Data Management, Statistics, and clinical teams.

This is an ideal opportunity for someone who enjoys SDTM governance, review, and strategic input, not just hands‑on programming.

Key Responsibilities

Provide expert oversight of SDTM programming activities from study start‑up through database lock and regulatory submission
Lead or review the development of submission‑ready CDISC SDTM packages, including aCRFs, define.xml, and cSDRGs
Review and contribute to trial set‑up documentation, including data transfer agreements, metadata, and trial design specifications
Create or review SDTM mapping specifications for internal and external data sources
Generate or oversee the creation of SDTM datasets using standardized conversion frameworks and utilities
Ensure high-quality, compliant datasets, including Pinnacle 21 review, readiness for interim analyses, medical review, and final lock
Program or oversee data quality checks and review reports to support Data Management and study teams
Maintain regulatory awareness, ensuring SDTM deliverables meet FDA, PMDA, and global submission requirements
Act as a subject matter expert across CDISC standards (SDTM, CDASH, controlled terminology, define.xml)
Support the development and implementation of programming standards within the organisation
At senior level: mentor junior or flexible resources and provide leadership or coordination of support teams where required

Key Interfaces

You will work closely with a wide range of stakeholders, including:

Clinical Programmers and Statistical Programmers
Clinical Trial and Data Management teams
Clinical Data Standards groups
External DM CRO partners
Enabling Business & Information Services (EBIS)

Required Experience & Skills

Bachelor’s degree (or higher) in Computer Science, Data Science, Mathematics, or a related scientific discipline (or equivalent experience)
Strong clinical programming background with hands‑on trial experience
Expert knowledge of SAS programming within a clinical research environment
Advanced expertise in CDISC SDTM, including aCRFs, define.xml, and cSDRGs
Deep understanding of clinical data structures (SDTM and working knowledge of ADaM)
Experience working in global, cross‑functional clinical research teams
Comfortable operating in a fast‑paced, matrixed FSP environment
Strong organisational, communication, and stakeholder management skills
Project oversight or coordination experience is highly desirable

Why Apply?

Long‑term stability through a strategic FSP partnership
Direct exposure to high‑impact regulatory submissions
Opportunity to operate as an SDTM standards and oversight expert, not just a producer
Collaborative, global environment with access to industry‑leading tools and standards
Clear pathway for senior technical influence and mentorship

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits

ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

Competitive base salary and performance related incentives
Health and wellbeing programmes including medical, dental, and vision coverage where applicable
Retirement and pension plans
Life assurance and disability coverage
Employee assistance programmes and wellbeing resources
Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility

ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request here.

Apply Now

Refine Your Search

pharmaceutical external jobs in dublin, d

Clinical SDTM Programmer

Pathology Project Manager

Supervisor, Laboratory

Maintenance & Calibration Lead

Global Supply Planner

Programme Director MSc in Procurement and Supply Chain Management

Senior Treasury Analyst

Senior Manager - Network Supply Planning

Capital Sales Specialist - Life Science, Ireland

Senior Specialist Regulatory Key Initiatives

Tech Transfer Lead, Drug Substance

Quality Engineering Manager

Associate, Contract Management

CNC Machinist

Director Respiratory Regulatory CMC

Quality Manager, Global Distribution Quality

Senior Manager - Network Supply Planning

Director of Network Pharmacy Contracting

Geo-Environmental Consultant

Treasury Manager/Senior Manager

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