Project Statistician Biomedicines in Madrid

or over 130 years, Lilly has been committed to the advancement of medicine and 
the development of innovative healthcare. Over 39,000 employees worldwide
are dedicated to the discovery, production and marketing of breakthrough drugs. 
These treat diabetes, cancer, sepsis, osteoporosis, erectile dysfunction,
 cardiovascular disease, disorders of the central nervous system and infectious diseases. In 2010 we invested roughly 5 billion US-$ in research and development.

Our European Statistics team works on a wide variety of projects covering early and late phases of drug development and market access. The European Statistics team provides innovative scientific and operational excellence in design, analysis, and interpretation in order to convert scientific information to knowledge that is useful to consumers and patients. The team is located on different sites across Europe.

We have been growing continuously for years. So why not grow with us?

Project Statistician Biomedicines (m/f)

Location: Germany (Bad Hamburg), UK (Erl Wood), France (Paris) or Spain (Alcobendas Madrid).

Best candidate will drive the decision.

The Project Statistician

    Is a successful problem solver who can use their technical expertise to work closely with other functions to answer important questions about our products by translating strategic needs to innovative statistical solutions

·         Is responsible for providing technical statistical consultancy to clinical trials, Observational Studies and other data-related research including data-mining projects in the Biomedicines area

·         Develops or assists in the development of clinical plans, protocol designs and statistical analysis plans in collaboration with physicians, health outcomes scientists and other medical/paramedical colleagues

·         Maintains an up-to-date knowledge of statistical methodology in order to maintain proficiency in applying new and varied methods and to be competent in justifying methods selected

·         Ensures high quality statistical support for projects through the oversight of CRO suppliers, and provide input into outsourcing strategy and processes

·         Assists with or is responsible for communicating study results via regulatory submissions, manuscripts, or oral presentations in group settings, as well as for communicating one-on-one with key customers and presenting at scientific meetings

·         Participates in peer-reviewing work products from other statistical colleagues

·         Performs work in full compliance with assigned curriculum(s) and will be responsible for following applicable corporate, medical, local, and departmental policies, procedures, processes, and training

Qualification; Experience

·         Msc or Ph.D. in Mathematics or Statistics, or equivalent experience

·         Excellent knowledge of statistical theory and methodology, with working knowledge of experimental design and statistics

·         Proficient in the SAS programming language

·         Strong self-management skills, excellent communication and presentation skills

·         Strong project management skills, business awareness/business development skills

·         Work effectively in geographically dispersed/virtual teams

·         Ability to manage work through third party interactions

·         Fluent in English – both oral and written

·         Pharmaceutical Experience is an advantage

If you know you can deliver the very best and wish to join us in taking on the challenges of the pharmaceutical business, then consider us. Your engagement will be remunerated with an attractive wage and above average social benefits. Your written application should convince us that we should getto know you personally. We look forward to hearing from you!