SAS Programmer

ppAt Recordati, we are united by a clear purpose: unlocking the full potential of life. With a century of history behind us, we are building the next chapter of our journey, continuing to grow while keeping patients at the centre of all we do. /p pWhat drives us is a shared belief that health, and the opportunity to live life to the full, should be within reach for everyone. This brings energy to our work, shaping how we support each other and show up every day. Our values – Better Together, Never Settle and Always Deliver – reflect this mindset, helping us to keep improving and make a meaningful difference. /p pAbove all, these values bring to life our promise to everyone at Recordati, you can unlock your full potential. We know that people thrive when they can be themselves, are trusted and supported, and are given the opportunity to grow and make a meaningful contribution. /p pAre you ready to unlock your full potential? /p h3Job Purpose /h3 pWe are looking for a Statistical Programmer that will be in charge of the programming of the output (tables, figures, listings) and generating the additional datasets related to the Company’s clinical studies on new drugs or marketed drugs by the Group’s companies followed by the CROs or directly including pooling of more studies. The person will improve and update the technical know-how about new programming techniques. /p h3Key Responsibilities /h3 ulliYou will program and validate the output (tables, listings and figures) to support the data cleaning and the statistical analyses required for clinical studies, publications, Regulatory and Market Access requests /liliYou will supervise the generation of the SDTM/ADaM datasets and related documents in compliance with CDISC guidelines as well as the output prepared by the CRO. /liliYou will develop standard SAS macros, templates and utilities and prepare the corresponding validation documents /liliYou will interact with the Statistician to prepare tables and listings according with the specification documents /liliYou will interact with the Data Manager in cleaning activities, external data management and reporting. /liliYou will interact with the Drug Safety Unit to evaluate the data from the pharmacovigilance database. /liliYou will lead efforts in the development, maintenance and adherence to divisional SOPs and guidelines. /li /ul h3Required Education /h3 pScientific degree (Statistics, Mathematics, Informatics) /p h3Required Skills And Experience /h3 p3-5 years of experience in a CRO or pharmaceutical company and clinical trials. /p pYou have a clear understanding of theoretical and applied statistic and regulatory guidelines in a pharmaceutical research setting; you are expert in the development and submission of NDA /p h3Technical Competencies /h3 pYou have knowledge of CDISC standards and preferably GCP. /p pYou know programming in SAS System. Optional R and/or SQL /p h3Required Behaviours And Competencies /h3 pYou are collaborative, good communicator and able to interact with all levels of the organization. /p h3Required Languages /h3 pFluent in English /p pAt Recordati we believe in people! Inspired by our purpose - unlocking the full potential of life - we are committed to creating a diverse environment and cultivating a culture of inclusion. We strive to continually lead with our values and beliefs, enabling our employees to bring their whole selves to work and develop their potential. /p pWe are proud to be an equal opportunity employer. We recruit, develop and reward without regard to, amongst others, gender, sexual orientation, gender identity or expression, national origin, age, physical or mental ability, race, ethnicity, political or religious belief. /p /p #J-18808-Ljbffr