Statistical Programmer

You will be joining an international and multi-cultural company that includes over 20 different nationalities with English as our working language. Our employees are our strongest asset. Our customers value our flexibility, responsiveness, and proactive approach.
By joining a group of 6 highly skilled Statistical Programmers, in the Biostatistical Services team of over 45 people, the successful candidate will strengthen the team in Raleigh, NC.

Your role:

As Statistical Programmer, you will collaborate on the analysis, interpretation and communication of clinical trials by creating statistical programs focused on data analysis and reporting. You will support the analysis of data gathered during the completion of clinical trials, including the tabulation of patient data and study findings.

Your responsibilities will be:

• Writing statistical programs for phase I to IV clinical trials following the Statistical Analysis Plan (SAP) and/or mock tables, including:
• Reading the protocol, eCRFs;
• Programming analysis datasets;
• Tabulating descriptive statistics using SAS macros;
• Running inferential statistics using SAS;
• Performing quality control of statistical programs;
• Modifying or writing new SAS programs and macros for greater analysis flexibility and increased automation of output production.

The successful candidate must have a university degree in mathematics, natural sciences or a health-related field and at least 2-3 years of experience in clinical trials research. In addition, the position requires:

• Knowledge of basic statistics.
• Knowledge of SAS.
• Knowledge of CDISC (ADaM).
• Knowledge of R and/or Python is an asset.
• Fluent in English, both written and oral.
• Detail-oriented with good time management skills.
• Good communication and organizational skills.
• Good problem-solving skills.
• Ability to work as a team player.