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Clinical Data Programmer

  1. Mexico City, Dublin, Johannesburg
JR114992
  1. Clinical Data Management, Programming, Clinical Programming
  2. ICON Full Service & Corporate Support

About the role

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Clinical Data Programmer

Location:

  • Mexico City
  • Dublin, Ireland
  • South Africa

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations.

With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life.

Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

We have an incredible opportunity for a Clinical Data Programmer (SDTM) to join the team.

Overview of the role:

The Clinical Data Programmer (CDP) is part of the Icon Medical Imaging Group, involved in clinical data receipt, programming and delivery. The CDP is responsible for supporting Clinical Data Programming Leads who serve as the lead on study specific programming set-up and delivery. The CDP is responsible for specifying, developing, validating, and executing programs and generation of clinical data deliverables.

  • Reviews database specification documents created by study teams, such as CRF Specifications and Data Delivery Specifications (DDS)
  • Creates/Programs edit checks, special actions, and derivations as per a DDS
  • Completes and maintains all study documentation as per ICON procedures
  • Completes study database updates as specified per Change Request documents and procedures
  • Trouble-shoots and solves study building issues and edit check programming issues
  • Reviews data set specifications per specified study requirements
  • Program and validate data sets
  • Create data programming specifications per specified study requirements
  • Program and validate clinical data programs

To be successful, you will need:

  • 1+ year(s) of experience in clinical data programming and delivery
  • Demonstrated ability to program clinical data deliverables
  • SDTM experience in a pharmaceutical setting
  • Ability to successfully handle multiple tasks and timelines
  • Team player with strong verbal and written communication skills
  • Advanced knowledge of the clinical data programming development life cycle
  • Competent knowledge of SAS programming
  • Ability to analyse, query and update relational databases using SQL
  • Bachelor’s degree in information systems, science or related discipline, or related experience required

Benefits of Working in ICON:

Our success depends on the knowledge, capabilities and quality of our people. That’s why we are committed to developing our employees in a continuous learning culture – one where we challenge you with engaging work and where every experience adds to your professional development.

At ICON, our focus is to provide you with a comprehensive and competitive total reward package that comprises, not only an excellent level of base pay, but also a wide range of variable pay and recognition programs. 

In addition, our best in class employee benefits, supportive policies and wellbeing initiatives are tailored to support you and your family at all stages of your career - both now, and into the future.

ICON, including subsidiaries, 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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