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Senior Statistical Programmer
A career at our company is an ongoing journey of discovery: our 60,300 people are shaping how the world lives, works and plays through next generation advancements in Healthcare, Life Science and Electronics. For more than 350 years and across the world we have passionately pursued our curiosity to find novel and vibrant ways of enhancing the lives of others.
United As One for Patients, our purpose in Healthcare is to help create, improve and prolong lives. We develop medicines, intelligent devices and innovative technologies in therapeutic areas such as Oncology, Neurology and Fertility. Our teams work together across 6 continents with passion and relentless curiosity in order to help patients at every stage of life. Joining our Healthcare team is becoming part of a diverse, inclusive and flexible working culture, presenting great opportunities for personal development and career advancement across the globe.
Under the supervision of a Project Statistical Programmer, you will perform trial and global project level programming across one or more clinical development programs. With direction, you will efficiently perform complex trial project level programming tasks, and without direction routine project and study level tasks, from set up to closure, within expected to high quality and project timelines. Specifically, you will apply the concept of strategic and defensive programming to daily work. With some guidance you will perform technical planning and oversight of programming to ensure efficient coding. In this role, you will provide solutions for programming tasks (including creation of macros), presenting alternatives and identifying the best solution.
Who you are:
- BSc or MSc (in a numerate discipline preferably in Statistics, Computer Science, or Mathematics)
- Proven success in a Statistical Programming role within clinical development at a pharmaceutical or biotech company, or at a CRO, equivalent to minimum of 4 years directly relevant experience.
- Proficiency in SAS (at least SAS/BASE, SAS/STAT, SAS/MACRO, SAS/GRAPH, SQL) and R programming
- Good knowledge of CDISC SDTM & ADaM (including specifications)
- Good understanding of processes associated with clinical trials
- Knowledge of statistical concepts
What we offer: With us, there are always opportunities to break new ground. We empower you to fulfil your ambitions, and our diverse businesses offer various career moves to seek new horizons. We trust you with responsibility early on and support you to draw your own career map that is responsive to your aspirations and priorities in life. Join us and bring your curiosity to life!
Curious? Apply and find more information at https://jobs.vibrantm.com