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ICON is a global healthcare intelligence and clinical research organisation united by a mission to bring new medicines and treatments to patients faster.
As a values-driven organisation, integrity, collaboration, agility, and inclusion are at the heart of how we work and interact with each other, customers, patients and suppliers.
As a Statistical Programmer II at ICON, you will the development, validation, and execution of statistical programs to support clinical trial analysis and reporting.
What You Will Do:
You will contribute to statistical programming activities, taking responsibility for your deliverables and working collaboratively.
Key responsibilities include:
Your Profile:
You will bring relevant statistical programming experience, along with the following qualifications and skills.
Required qualifications and experience:
4+ years of experience developing broad solutions in SAS across clinical programs or a therapeutic area
SDTM submission experience including Define.xml, CDASH, and metadata as well asexperience transforming transferred vendor data into SDTM preferred, knowledge of ADaMa plus
Demonstrated understanding of current industry standards for submission of clinical trialdata.
Employment with ICON is contingent upon having the legal right to work in the country where the role is based.
Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.
Benefits may include:
Benefits may vary depending on role and location.
Visit our to read more about the benefits ICON offers.
Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.
If you require reasonable accommodations during the recruitment process, please let us know or submit a request.
Are you a current ICON Employee Please click to apply
Since our foundation in Dublin, Ireland in 1990, our mission has been to help our clients to accelerate the development of drugs and devices that save lives and improve quality of life. We do this by delivering best in class information, solutions and performance, with an unyielding focus on quality at all times.We offer a full range of consulting, development and commercialisation services from a global network of offices in 37 countries. We focus our innovation on the factors that are critical to our clients – reducing time to market, reducing cost, and increasing quality – and our global team of experts has extensive experience in a broad range of therapeutic areas.
Job ID: 148152291
Skills:
cdisc standards , Sas Programming, statistical programming, Regulatory Requirements
Skills:
SAS, Python, R, R-Shiny, Statistical methodologies, Clinical data management systems
We don’t charge any money for job offers