Statistical Programmer – SAS M/F

You are a highly skilled professional with passion for the world of life sciences and clinical research? You want to thrive in a dynamic and collaborative international environment where your expertise directly impacts people lives? Come and join Aixial Group to contribute to shaping the future of clinical research!Who Are we?We are one of the world’s leaders in CRO (Contract Research Organisation) with the commitment, expertise, and flexibility needed to deliver efficient clinical trials.We work with global pharmaceutical, biotech, cosmetic, medical device, and many other companies around the globe, providing them with innovative and scalable solutions.We are operating in 10 countries across 3 continents, bringing together over 1000 talented professionals dedicated to make a positive impact in the life sciences industry.We have been part of ALTEN Group since 2014 and are continuously exploring new opportunities to expand our activity worldwide.Why Join Us? Make a positive impact and be at the forefront of project  : You will be part of groundbreaking advancement in clinical research that has positive impacts on millions of people’s lives globally.People are our biggest asset. We are committed to empower our team continually and build a positive and supportive environment that fosters growth, flexibility, and teamwork. At Aixial Group, you will be coached and mentored throughout your journey to help you advance your professional and personal growth. Our commitment to Diversity, Equality, and Inclusion  :We aim to create a workforce which promotes dignity and respect, where individual differences are recognized and valued, and where each employee can give their best.Gender equality is at the core of the development strategy of Aixial Group.Aixial Group continues to grow, and to recruit in the clinical trial professions. Join us, and discover our website to follow the news of our offers: https://www.aixialgroup.com/join-us/AIXIAL Group is looking for its next talented Statistical Programmer – SAS M/F. Your tasks will include (but are not limited to) :Define and develop biostatistical methodologies for clinical studiesCalculate the number of subjects and write the statistical part of the protocolDesign the statistical analysis planSelect a statistical model and define the statistical methodology for clinical studiesAnalyse and interpret the statistical results of clinical studiesCreate the statistical analysis planParticipate in drafting and validating the protocolDraw up randomisation plansValidate the evaluation criteriaCarry out and program statistical analysesWrite statistical sections of study reportsPresent statistical resultsDevelop code documentation in SAS programmingDesign and program analysis datasets (CDISC)Test and validate the programsProgram tables, listings and graphs according to the statistical analysis planManage and update the program libraryProfile and skills required :You have a Master or Engineer degree in clinical research, statistics, mathematics or equivalentYou have at least 5 years experience as a biostatistician in clinical trialsYou must have experience in SAS programmingKnowledge of R would be a plusYou have experience working in a pharmaceutical laboratory and/or CROYou have knowledge of : CDISC – CDASH – ADAM – SDTMYou are fluent in written and spoken English and French would be a plusYou have a sense of responsibility and rigorYou are independent, proactive and organised Belgium Denmark France Germany Portugal Romania Spain United Kingdom Belgium Denmark France Italy Portugal Romania Spain #J-18808-Ljbffr