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This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. Our Senior Statistical Programmers play a key role within ICON developing and executing statistical programs designed to analyze clinical trial information.

The Senior Statistical Programmer will be responsible for designing and developing standard software and data structures, developing and executing statistical programs designed to analyze clinical trial information and participating in the development and maintenance of SOPs (including software validation, documentation, study archiving and others as needed). The Senior Statistical Programmer will also be responsible for Leading programming deliverables and programming teams, effective resource planning, project tracking, ensuring project, timeline and quality goals are consistently achieved, effectively liaising with other functions in the conduct of programming activities, and also working in a sponsor facing lead role. This position can be based in the UK, Ireland or Central Europe, with potential for home-based working.

Overview of the role

Develop and execute statistical analyses of clinical trial data. Design and develop computer programs that produce tables, figures, listings and derived datasets that summarize results of clinical trials.
Participate in the review of Case Report Forms (design phase), Statistical Analysis Plans, QC Specifications and Database Structures.
Assess data from clinical trials for consistency and accuracy.
Develop and implement quality assurance software.
Design and implement analysis file structures.
Monitor procedures for software validation.
Work on cross-disciplinary teams to assure programming needs are met and appropriate requests are made.
Leading programming deliverables and programming teams
Sponsor facing lead role

Role Requirements

Bachelors of Science degree in a quantitative discipline (or training equivalent to) or equivalent work experience.
8+ years full time SAS programming experience for Senior Programmer; experience must be in the pharmaceutical or biotechnology industry.
Understanding of data structures, standard software and their implementation.
Knowledge of the drug development process (Phase I through IV) and general regulatory requirements.
Good written and verbal communications skills
Prior oncology experience preferable

If you are looking to join a company which will offer you a strong support network and an inspiring working environment, then this is the job for you. Applicants must be able to demonstrate drive, passion and a strong sense of team working, along with a desire to progress within our organisation. Successful candidates will also have great communication, both verbal and written.

In return, we offer a strong benefits package that includes comprehensive health and pension plans, competitive salary, holidays, and an incentive plan for strong performers.

*LI-AC1

A better career. A better world. A better you.

Our people are our greatest strength, are the core of our culture and the driving force behind our success. Throughout all levels of the company, our people have a drive to succeed and a passion that ensures what we do, we do well. We help you build exciting and rewarding careers, deliver results to help bring life-changing medicine and devices to market and maintain ICON’s success as an industry leader.
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Sr Statistical Programmer I

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