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Associate Principal 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 function as the EC Lead Statistical Programmer for one or more clinical trials and/or other global project sub tasks, across one or more clinical development programs. Specifically, you will be responsible for the statistical programming deliverables according to defined project timelines and quality expectations to achieve project goals. You will coordinate basic statistical programming aspects of trials or other project subtasks and can lead standard subtasks. Additionally, you can independently develop, validate, troubleshoot, and maintain complex programs in accordance with defined specifications and standards. In this role, you will provide expert statistical programming advice, guidance, and training to junior trial team members. In addition, you may contribute to departmental innovation and process improvement projects.
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 6 years directly relevant experience.
Proficiency in SAS (at least SAS/BASE, SAS/STAT, SAS/MACRO, SAS/GRAPH, SQL) and R programming
In-depth understanding of clinical data structure (e.g. CDISC SDTM & ADaM standards including specifications, Define.xml and ADRG)
Excellent understanding of processes associated with clinical trials
Good knowledge of relevant regulatory guidelines
Good Knowledge of statistical concepts
Demonstrated project management skills.
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