Associate Clinical System Designer

Posted 6 Days Ago
Be an Early Applicant
Swansea, Wales, GBR
In-Office
Entry level
Healthtech • Biotech • Pharmaceutical • Manufacturing
The Role
Supports the design, configuration, testing, maintenance, documentation, and quality assurance of clinical trial systems. Collaborates with cross-functional teams to translate study requirements into system setups, assists users with troubleshooting, contributes to process improvements, and helps produce clinical trial metrics and reports. The role is designed for graduates and includes structured training in clinical research technology and data management.
Summary Generated by Built In
Associate Clinical System Designer- Swansea

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.


Are you interested in clinical research, technology, or data? Join ICON as an Associate Clinical Systems Designer and help build and maintain the systems that support the development of life-changing medicines.

This is an excellent opportunity for graduates looking to develop a career at the intersection of clinical research and technology. You will receive training, work alongside experienced professionals, and gain exposure to how clinical trials are managed from a systems and data perspective.

What You Will Do:

As an Associate Clinical Systems Designer at ICON, you will support the setup, testing, and maintenance of the systems used to manage clinical trial data. Working alongside experienced colleagues, you will help ensure these systems are configured correctly, perform as expected, and support the successful delivery of clinical studies.

Key responsibilities include:

  • Assisting with the design, configuration, and testing of clinical systems used to collect and manage clinical trial data

  • Working with cross-functional teams to understand study requirements and ensure systems are set up to support clinical trial needs

  • Supporting system testing, documentation, and quality checks to ensure compliance with industry and regulatory standards

  • Providing support to system users and helping troubleshoot system-related issues

  • Contributing to process improvements and system enhancements that improve efficiency and user experience

  • Supporting the delivery of clinical trial metrics and reports that help teams monitor study progress

You will have/be:

  • A Bachelor's degree in Life Sciences, Health Sciences, Computer Science, Information Systems, Data Analytics, or a related discipline

  • An interest in clinical research, healthcare technology, or data management

  • Strong analytical and problem-solving skills with excellent attention to detail

  • Good communication and collaboration skills, with the ability to work effectively across different teams

  • The ability to learn new technologies and adapt in a fast-paced environment

  • Experience with clinical systems, databases, or technology platforms would be beneficial but is not essential

#LI-RD1


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 Life Sciences, Health Sciences, Computer Science, Information Systems, Data Analytics, or a related discipline
  • Interest in clinical research, healthcare technology, or data management
  • Strong analytical and problem-solving skills
  • Excellent attention to detail
  • Good communication and collaboration skills
  • Ability to learn new technologies and adapt in a fast-paced environment
  • Experience with clinical systems, databases, or technology platforms

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.

  • 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.
  • 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.
  • 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

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The Company
HQ: Dublin
34,685 Employees
Year Founded: 1990

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.

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