Office based or remote working

Locations: UK, Poland, Bulgaria, Romania, Estonia, Lithuania

We are the global Real World Evidence Strategy and Analytics team dedicated working on observational and real world evidence based trials for a number of indications.

As a Statistical Programmer II you will develop statistical analysis plans and perform statistical analysis on assigned projects in accordance with study specifications, applicable guidelines, regulatory requirements and SOPs. Project responsibilities include study design, case report form development, analysis planning and scheduling, analysis and interpretation of data, and reporting of results. May be required to coordinate analysis efforts across multiple research projects conducted for a clients:

You will be expected to recognize the importance of and build a culture of process improvement with a focus on streamlining our processes adding value to our business and meeting clients’ needs.

Key responsibilities will include:

• Responsible for preparing and reviewing Statistical Analysis Plans including table and listing shells

• Researching up-to date therapeutic statistical methods

• Executing statistical models, using SAS

• Responsible for programming and Quality Control of statistical analyses

• Performing ad-hoc and exploratory analysis of data

• Reviewing and QC SAS output for consistency with Statistical Analysis Plan

• Responsible for participating in data validation process

• Responsible for generating and review randomization lists

Requirements:

• Master's Degree in Statistics, Biostatistics

• Minimum 4+ years of Statistician experience in a biotechnology, pharmaceutical, CRO or other health care setting

• Knowledge of basic and advanced and emerging statistical research designs and methodologies in clinical and epidemiological research

• Strong SAS programming skills and understanding of database structures

• Ability to use structured programming techniques

• Ability and willingness to use and/or modify existing programs and macros

Benefits of Working in ICON:

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.

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,
 

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