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.
As a Senior Clinical System Designer at ICON, you will design and implement advanced clinical systems that enhance trial design and execution.
What You Will Be Doing:
Develop, validate, and maintain programming solutions for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials.
Collaborate with data managers, project managers, clinical data scientists, and biostatisticians to ensure the integration of programming solutions into the overall data management process.
Act as a primary point of contact during the study set up and maintenance phase for system programming related questions by the project team.
Support colleagues with the clinical trials environment and concepts of Clinical Data Management Systems.
Perform extracts of data from CDMS and creation of data transfer programs.
Act as mentor and provides guidance and support to more junior programmer levels assigned to a project.
Assist in the development and implementation of improvements to technical systems and processes within an SME role.
Provide guidance on programming best practices, coding standards, and data quality control measures.
Stay updated on advancements in programming languages and data management tools to enhance operational efficiencies.
Your Profile:
Complete bachelor’s degree relevant field such as computer science, SAS, statistics, or life sciences.
Extensive experience in programming for CDMS (EDC systems such as Rave/Veeva), data validation outputs, data review/risk management outputs, custom reports, and programs in clinical trials with proficiency in languages such as SAS, R, or Python.
Strong problem-solving skills and the ability to work collaboratively in a fast-paced, cross-functional environment.
Excellent attention to detail and organizational skills, with a commitment to delivering high-quality results.
Strong communication and interpersonal skills, with the ability to effectively collaborate with diverse teams and influence outcomes.
MUST HAVE advanced English Communication, Writing and Reading
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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.
Are you a current ICON Employee? Please click here to apply
Skills Required
- Bachelor's degree in computer science, statistics, life sciences, or relevant field.
- Extensive experience programming for CDMS/EDC systems (e.g., Rave, Veeva).
- Proficiency in SAS, R, or Python for clinical trial programming.
- Experience performing data extracts and creating data transfer programs from CDMS.
- Knowledge of data validation outputs, data review/risk management outputs, and custom reporting in clinical trials.
- Ability to mentor and provide guidance to junior programmers.
- Advanced English communication, writing, and reading skills (MUST HAVE).
- Familiarity with clinical data management systems and clinical trials processes.
ICON plc Compensation & Benefits Highlights
The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about ICON plc and has not been reviewed or approved by ICON plc.
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Healthcare Strength — Benefits are described as comprehensive, with medical coverage and wellness initiatives highlighted. Larger sites are also associated with added wellness supports such as onsite fitness options and access to an employee assistance program.
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Leave & Time Off Breadth — Time-off and flexibility provisions are positioned as a meaningful part of the total package, including vacation/annual leave and flexible work scheduling. Flexibility is sometimes cited as helping offset long hours in certain roles.
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Retirement Support — Retirement and savings support is presented as a core component of the benefits package, including offerings such as pension arrangements in some locations and a U.S. 401(k) plan with company match. Financial planning resources are also emphasized as part of broader security benefits.
ICON plc Insights
What We Do
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times. We offer a full range of consulting, development and commercialisation services from a global network of offices in 53 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
