Clinical Data Standards Architect
- France, Germany, Poland, Spain, UK
- Programming
- ICON Strategic Solutions
- Home-Based
TA Business Partner
- Icon Strategic Solutions
About the role
Are you passionate about clinical data standards and looking to make a meaningful impact in the world of clinical research? Join our dedicated global team as a Clinical Data Standards Architect, where you’ll play a key role in streamlining clinical data processes across therapeutic areas. This role is integral to ensuring high-quality data collection and delivery, aligning with industry standards and regulatory requirements.
You will be at the forefront of developing, implementing, and maintaining standard metadata, supporting the full data lifecycle from initial collection to final submission.
You will:
Implement standard content in data collection and delivery tools, driving consistency, automation, and efficiency across clinical trials.
Configure standards for specific Therapeutic or Disease Areas to enable optimal reuse and adoption across the R&D portfolio.
Collaborate with cross-functional teams, including data managers, technical architects, and standards experts, to ensure the correct configuration and adoption of clinical data standards.
Ensure compliance with industry standards (e.g., CDISC) and health authority regulations, incorporating best practices in computer system validation.
Conduct testing and quality control of tools, mapping metadata, and standard implementations.
Maintain and govern master-level data collection and delivery standards, applying formal change control and versioning practices.
Support lineage and traceability documentation for all pre-configured standards used across studies.
Provide subject matter expertise to internal teams and external partners (e.g., CROs) on the adoption and implementation of clinical data standards.
Develop and maintain standard CRF mockups, questionnaires, validation rule specifications, and integrations (e.g., IWRS).
Education & Experience:
Bachelor’s degree in Life Sciences, Computer Sciences, or equivalent experience.
Minimum of 2 years’ relevant operational experience in clinical data management or data standards.
Technical Skills:
- Strong expertise in Rave eDC (Medidata Solutions).
- Experience with SAS programming; coding skills preferred.
- In-depth understanding of CDISC standards: SDTM, CDASH, define.xml, and Controlled Terminology.
- Familiarity with SAS LSAF and Pinnacle 21 is advantageous.
- Ability to manage multiple priorities effectively in a matrixed environment.
Soft Skills:
Excellent communication skills, both written and verbal, in English.
Strong collaboration mindset with the ability to work across global teams and stakeholders.
High attention to detail and a structured, analytical approach to problem-solving.
What ICON can offer you:
Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.
In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.
Our benefits examples include:
- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs
- Competitive retirement planning offerings to maximise savings and plan with confidence for the years ahead
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others
Visit our careers website to read more about the benefits of working at ICON: https://careers.iconplc.com/benefits
At ICON, inclusion & belonging are fundamental to our culture and values. We’re dedicated to providing an inclusive and accessible environment for all candidates. ICON is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, colour, religion, sex, sexual orientation, gender identity, national origin, disability or protected veteran status. If, because of a medical condition or disability, you need a reasonable accommodation for any part of the application process, or in order to perform the essential functions of a position, please let us know through the form below.
https://careers.iconplc.com/reasonable-accommodations
Interested in the role, but unsure if you meet all of the requirements? We would encourage you to apply regardless – there’s every chance you’re exactly what we’re looking for here at ICON whether it is for this or other roles.
#LI-JF1
Impactful work. Meaningful careers. Quality rewards.
At ICON, our employees are our greatest strength. That’s why we are committed to empowering you to live your best life, both inside and outside of work. Whether your ambition is lead a global team, become a deep scientific or technical expert, work in-house with our customers or gain experience in a variety of different ICON functions, we will support you in realising your full potential. See all locations Learn more about Our Culture at ICON
Day in the life
Similar jobs at ICON
Salary
Location
Canada
Department
Biometrics Roles
Location
Canada
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Programming
Job Type
Permanent
Description
A Patient Reported Outcome (PRO) is a direct measurement of how a patient survives, feels or functions as a result of disease/illness and/or treatment. PRO feedback is always from the patient's (or ca
Reference
2025-122134
Expiry date
01/01/0001
Author
Kala MurphyAuthor
Kala MurphySalary
Location
Taiwan, Taipei
Location
Taipei
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Senior Statistical Programmer (all levels) to join our diverse and dynamic team. As a Statistical Programmer at ICON, you will play a crucial role in analyzing clinical tria
Reference
JR134672
Expiry date
01/01/0001
Author
Huixin "Stella" SongAuthor
Huixin "Stella" SongSalary
Location
India, Bangalore
Location
Bangalore
Bengaluru
Remote Working
Office or Home
Business Area
ICON Strategic Solutions
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Senior Statistical Programmer I to join our diverse and dynamic team. As a Senior Statistical Programmer I at ICON, you will play a crucial role in analyzing clinical trial
Reference
JR134546
Expiry date
01/01/0001
Author
Himangshu Skekhar DasAuthor
Himangshu Skekhar DasSalary
Location
Argentina
Department
Biometrics Roles
Location
Argentina
Remote Working
Home-Based
Business Area
ICON Strategic Solutions
Job Categories
Programming
Job Type
Permanent
Description
A Patient Reported Outcome (PRO) is a direct measurement of how a patient survives, feels or functions as a result of disease/illness and/or treatment. PRO feedback is always from the patient's (or ca
Reference
2025-122188
Expiry date
01/01/0001
Author
Magda ObregonAuthor
Magda ObregonSalary
Location
Romania, Bucharest
Location
Paris
Bucharest
Madrid
Reading
Mannheim
Remote Working
Remote
Business Area
ICON Strategic Solutions
Job Categories
Clinical Data Scientist Lead
Clinical Programming
Job Type
Permanent
Description
We are currently seeking a Visualization Developer to join our diverse and dynamic team. As a Visualization Developer at ICON Strategic Solutions, you will be instrumental in leading the development a
Reference
JR134568
Expiry date
01/01/0001
Author
Niki ScottoAuthor
Niki ScottoSalary
Location
UK, Swansea
Location
Swansea
Remote Working
Office Based
Business Area
ICON Full Service & Corporate Support
Job Categories
Clinical Programming
Job Type
Permanent
Description
We are currently seeking an Associate Clinical Data Science Programmer to join our diverse and dynamic team. As an Associate Clinical Data Science Programmer at ICON, you will be instrumental in devel
Reference
JR133910
Expiry date
01/01/0001
Author
Rowena DeswertAuthor
Rowena Deswert