Company DescriptionWe are the company that cares – for our staff, for our clients, for our partners and for the quality of work we do.
A dynamic, global company founded in 1995, we bring together more than 2,700 driven, dedicated and passionate individuals.
We work on the frontline of medical science, changing lives, and bringing new medicines to those who need them.Job DescriptionYou will contribute to statistical programming activities related to global clinical trials, work closely with international teams of statisticians, programmers and data managers, program data sets and summaries.You will:Develop analysis data sets structureDevelop program requirements and specificationsBe involved in SAS programming of ADS and Tables, Listings and FiguresSupport SAS program validationsPrepare and review program documentationProduce TFLCommunicate with project teams and company departments with regard to statistical programming of clinical research projectsQualificationsUniversity and master's degree in applied science, mathematics, statistics or the likeKnowledge of SAS software (SAS BASE/SAS STAT/SAS GRAPH) and experience of work in SAS systemGood knowledge of programming logic, SQL and macro programming is preferredProficient in English, spoken and writtenExperience within clinical trials and/or BiostatisticsGood analytical skillsProficiency in standard MS Office applicationsExcellent communication and interpersonal skillsPlease submit your CV in EnglishAdditional InformationOur mission is to be the best CRO in the world as measured by our employees, clients, sites, and vendors.
Our recruitment process is easy and straightforward, and we'll be there with you every step of the way.
Having recently been awarded five CRO Leadership Awards in 2021, this is a great time to be joining a well-respected, Global company.Seniority levelAssociateEmployment typeFull-timeJob functionOtherIndustriesPharmaceutical Manufacturing
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