Senior Biostatistician

4 days ago

Shefford, Central Bedfordshire, United Kingdom ICON Plc Full time
Statistical Programmer II Role at ICON Plc

ICON Plc is a leading healthcare intelligence and clinical research organization, dedicated to fostering an inclusive environment that drives innovation and excellence. We invite you to join our mission to shape the future of clinical development.

The Role:

Our global biostatistics team is responsible for medical device and late-phase research, working on peri and post-approval research, post-authorization safety studies, observational and non-interventional studies, patient-reported outcomes, and analyses for abstracts, papers, and manuscripts.

As a Statistical Programmer II, you will be responsible for the statistical aspects of clinical and preclinical research projects. Your project responsibilities will include study design and case report form review, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. You may be required to coordinate analysis efforts across multiple research projects conducted for a client.

You will have strong demonstrable experience in:

  • Designing, developing, validating, and documenting SAS programs to generate analysis datasets, summary tables, figures, and listings.
  • Supporting statisticians in the development and review of Statistical Analysis plans and programming specifications.
  • Assisting data management with implementing CRFs.

We are looking for:

  • Bachelor's or Master's degree in statistics, biostatistics, or a related field.
  • SAS programming experience (ideally 3 years or more).
  • Major experience in the Pharmaceutical/CRO industry.

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