The main purpose of the role is to develop and standardise (re-usable) program code for the purpose of undertaking data validation, and for generating tables, listings and figures (TLFs) which are part of interim and final clinical study reports.
Qualifications required are a degree in either Biostatistics, Computer Science, or Life Sciences with demonstrated programming experience in the fields of biostatistics and/or pharmacometrics. A minimum of 2 years' relevant work experience and an understanding of drug development industry, its processes and regulations. A high level of proficiency using, SAS® software, R (open source), and other statistical analysis or data visualization software packages. Experience in CDISC Standards and / or experience in clinical data management is advantageous.
In return, CNS offers the successful candidate an opportunity to work in a highly client orientated, rapidly growing service company within a responsive, internationally experienced team, whose goal is to provide committed, passionate and innovative clinical research support and solutions to our clients, our research sites and our partners.
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