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Clinical Data Programming Lead (SAS)

North Wales,Mexico City,Canada
Permanent
Reference: JR071013
Description

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 a Clinical Data Programming Lead to join the team.

Location Options:

  • United States (home-based OR office-based)
  • Mexico (office-based with some remote flexibility)
  • Canada (home-based OR office-based)

Summary:

This Clinical Data Programming Lead (CDPL) is part of the Clinical Data Services (CDS) group involved in clinical data receipt, programming and delivery. The CDPL is responsible for overseeing the set-up and maintenance of clinical data deliverables on multiple clinical studies.

The CDPL participates in activities as related to the specification, validation and quality assurance of study data deliverables and applies competent experience and knowledge in support of the clinical data programmers assigned to a clinical study.

Highlights of Key Responsibilities:

  • Serves as the clinical data delivery lead on multiple study specific programming setup, leading clinical data programming activities on multiple studies
  • Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets.
  • Plans and works with the clinical programming group to schedule specification, programming, validation and ongoing delivery activities. Manages timelines for programming setup process, ensures issues are addressed in a timely manner to meet timelines and produces clinical data delivery validation packages for delivery.
  • Co-ordinates and manages study database updates and out of scope impacts as specific per Change Request documents and procedures.

Requirements:

  • Ideal background is 4+ years of experience in clinical data programming, but candidates with 1+ years will be considered
  • Proven SAS programming experience
  • Experience with clinical data programming and the ability to review and evaluate clinical data
  • Demonstrated ability to produce CDISC and Sponsor defined clinical data deliverables
  • Successfully handle multiple tasks and timelines
  • Team player with strong verbal and written communication skills
  • Bachelor's degree in information systems, science or related discipline or meaningful experience required

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.

 

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