ICON Clinical Research

Clinical Data Programming Lead

Expiring today

Location
Leuven
Salary
Competitive
Posted
22 Feb 2021
Closes
26 Feb 2021
Ref
JR070084
Hours
Full Time
Contract Type
Permanent
Experience Level
Experienced (non-manager)
At ICON, it's our people that set us apart. Our diverse teams enable us to become a better partner to our customers and help us to fulfil our mission to advance and improve patients' lives.

Our 'Own It' culture is driven by four key values that bring us together as individuals and set us apart as an organisation: Accountability & Delivery, Collaboration, Partnership and Integrity. We want to be the Clinical Research Organisation that delivers excellence to our clients and to patients at every touch-point. In short, to be the partner of choice in drug development.

That's our vision. We're driven by it. And we need talented people who share it.
If you're as driven as we are, join us. You'll be working in a dynamic and supportive environment, with some of the brightest and the friendliest people in the sector, and you'll be helping shape an industry.

We have an incredible opportunity for an expert Clinical Data Programming Lead to join the team.

The Role:

  • Role is located at sponsor's site as part of a tightly knit ICON global team


  • Full initial On-boarding and continuous support provided


  • Planning and working with the data management and clinical programming group to schedule specification, programming, validation and ongoing delivery activities.
  • Ability to write and execute SAS programs to produce internal and Sponsor deliverables. Programming is based in CDISC Standards
  • Leads timelines for programming setup process, ensuring issues are addressed and producing clinical data delivery validation packages to the study teams to file in the Trial Master File.
  • Participates in activities related to the specification review, program validation and quality assurance of study data deliverables, applying expert experience and knowledge to support the clinical data programmers assigned to a clinical study.


* Attends sponsor audits, including presenting the Clinical Data Delivery process and procedures from a compliance perspective.

You will need:
* Degree in a Technical or Science background coupled with strong experience in Clinical Data Management and SAS programming.
* Ability to work to tight deadlines and effectively run multiple projects to specific client requests
* Strong communication skills as you will be working across a highly matrix organisation internally and externally.

Benefits of Working in ICON:
Our success depends on the quality of our people. That's why we've made it a priority to build a culture that rewards high performance and nurtures talent.

We offer very competitive salary packages. And to keep them competitive, we regularly benchmark them against our competitors. Our annual bonuses reflect delivery of performance goals - both ours and yours.
We also provide a range of health-related benefits to employees and their families and offer competitive retirement plans - and related benefits such as life assurance - so you can save and plan with confidence for the years ahead.
But beyond the competitive salaries and comprehensive benefits, you'll benefit from an environment where you are encouraged to fulfil your sense of purpose and drive lasting change.

ICON is an equal opportunity and inclusive employer and is committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, 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.