Senior Clinical Data Programmer

hace 2 semanas

Desde casa, Colombia ICON A tiempo completo
ICON plc is a world-leading healthcare intelligence and clinical research organization.

From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organizations.


With our patients at the center 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
Senior Clinical Data Programmer (SAS) to join the team.

Location:
home-based OR office-based

  • United States
  • Canada
  • Mexico
  • Colombia

Overview of the role:

The Senior Clinical Data Programmer (Sr. CDP) is part of the Clinical Data Services (CDS) group involved in clinical data receipt, programming and delivery.

The Senior CDP responsible for supporting Clinical Data Programming Leads who serve as the lead on study specific programming set-up and delivery.

The Senior CDP is responsible for specifying, developing, validating, and executing programs and generation of clinical data deliverables. Additionally, the Senior CDP is responsible for QC of less experiences programmer deliverables and assisting with project management.

  • Annotate CRFs in accordance with CDISC published or sponsor specific guidelines with appropriate metadata to reflect case report tabulation (CRT) data sets
  • Create 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
  • Review and quality assure CRF, data set and programming specifications, program code and outputs
  • Execute programs and generate clinical data outputs according to study/client requirements
  • Manage multiple projects, ensuring that timelines are met and deliverables are of sufficient quality
  • Provide ongoing support, mentorship and training as appropriate, to members of the team involved in data operations and delivery.

To be successful, you will need:

  • 4+ year(s) of experience in clinical data programming and delivery
  • Demonstrated ability to produce programmed clinical data deliverables
  • 4+ years of SAS experience in a pharmaceutical setting
  • Advanced knowledge of SAS programming
  • Ability to liaise professionally with team members
  • Knowledge of the clinical data programming development life cycle and programming concepts
  • Associates 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.
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