We 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 ****, 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 willcontribute to statistical programming activities related to integral clinical trials, work closely with international teams of statisticians, programmers and data managers, program data sets andsummaries.You will:Develop analysis data sets structureDevelop program requirements and specificationsBe involved in SAS programming of ADS and Tables,



Listings and FiguresSupport SAS program validationsPrepareand review program documentationProduce TFLCommunicatewith project teams and company departments with regard to statistical programming of clinical research projectsQualificationsUniversityandMaster'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 system is desirableGood knowledge of programming logic, SQL and macro programming is preferredProficient inEnglish, spoken and writtenExperience within clinical trials and/or BiostatisticsGood analytical skillsProficiency in standard MS Office applicationsExcellent communication and interpersonal skillsAdditional 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.
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📌 Sas Programmer I (Buenos Aires)
🏢 Psi Cro
📍 Buenos Aires