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Clinical Data Programmer - Wavre, Belgium

ICON is proud to announce the new partnership with one of the top Pharma's in Europe. Both organisations join together with a strong science and technology focus to deliver best in class solutions to the healthcare industry.

As the Clinical Data Programmer you will participate in the data management technical aspects of Clinical or Epidemiological studies which includes the development of specific tools to collect, monitor, clean and report study data.

About Clinical Data Programmer at ICON:

In this central role, you will be responsible for supporting CDMS Programming activities as related to building study databases, system reports and configuring other system features. As a Clinical Data Programming Lead you can also function as a Team Lead for CDMS Programmers, ensuring team delivers to expected quality and timelines and providing technical oversight and training/mentoring.

Responsibilities:

Participates in study specific database set-up within at least one CDMS system (preferred Inform).
Reviews database specification documents created by study teams, such as CRF Specifications and Data Validation Specifications (DVS)
Creates/Programs edit checks, special actions and derivations as per a DVS.
Works closely with centralized CDMS Testing Group to ensure all programming issues are resolved in a timely manner and study timelines are met
Trouble-shoots and solves study building issues and edit check programming issues.
Serves as Team lead to CDMS Programmers, providing training, best practices, support and quality checks on study build and programming; ensure effective resource allocation and workload balancing across assigned team members
Extend technical expertise and mentor team members on an ongoing basis; ensure team achieves productivity and quality targets, perform benchmarking reviews and perform oversight of deliverables using different tools/ techniques and maintain and report relevant metrics.
Contributes to training materials on a process, system or technology level. Works with CTD and CDMS Management on delivery of training courses, instructor-led and on-the-job.

To succeed you will need:

The successful individual will have a proven experience in study build set up; possess a strong understanding of the principles of system development lifecycle and governance and be able to perform assigned tasks with minimum supervision.

Prior relevant experience in building study databases
Ability to successfully manage multiple tasks and timelines
Experience in Medidata Rave or other EDC system
Team player with strong verbal and written communication skills
Demonstrated ability to learn new technologies, applications and techniques
Understanding of database concepts.

Application process

Once you find a job opening that fits your skills and interests, you can create an account, apply and check back on the progress of your application or apply for other roles. Once your application has been received, a confirmation email will be sent to your email.

Remember: this is our first time meeting you. Read the job description and highlight on your CV those experiences that we should learn about.

One of our experienced recruiters will read your profile and determine if you're fit for the role and the company. We are aware of instances where fake recruitment text messages and emails that can appear to come from ICON have been received by individuals. Always delete suspicious text messages or emails. Never give out personal financial information.

Reasonable Accomodations

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Clinical Data Programmer

About the role

This vacancy has now expired. Please see similar roles below...

ICON and you

ICON history

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Benefits & Rewards

DE&I

Environmental, Social & Governance

Women in IT

Application process

Who we are

Government and public health services

Why icon? full service mean for you?

Clinical Data Programmer

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About the role

This vacancy has now expired. Please see similar roles below...

ICON and you

ICON history

Career Pathways

Benefits & Rewards

DE&I

Environmental, Social & Governance

Women in IT

Application process

Who we are