Non-Clinical Statistician
12 month rolling contract
Mainland Europe
Job Summary:
Your primary responsibility will be to work as a statistician in the non-clinical research and development of new drugs, as well as in the quality and process control of pharmaceutical manufacturing. The position involves working closely with other statisticians, programmers, biologists, pharmacists and physicians.
Accountabilities/Responsibilities:
* Planning and decision making for state-of-the-art study designs, evaluating methods and performing sample size calculations for the units of Respiratory, CNS, Oncology and Cardiovascular Research, Analytical Development and Nonclinical Drug Safety
* Consulting and guidance of biologists in statistical questions
* Responsibility for study evaluation and reporting
* Implementation of statistical methods for quality assurance and process control in pharma manufacturing
* Discussing statistical issues with drug regulators
* Statistical training of lab heads and lab personnel
Essential Skills & Capabilities:
You will be expected to have an MSc or PhD degree in statistics or mathematics as well as a comprehensive knowledge of biostatistics. You should also be familiar with the application of new statistical methods and theories in software solutions involving SAS or R. Experience as a statistician in non-clinical research and development is considered a major advantage.
Personally you are self-motivated, a good communicator and team player, you are fluent in English and enjoy working on challenging scientific projects and studies in an international setting
For a confidential consultation call Harry Withenshawe on 0044 (0) 207 255 6665 or email your CV to [log in to unmask]
Harry Withenshawe
Associate Consultant
Statistics, Biostatistics & Programming
Tel: +44 (0) 207 255 6665
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Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician
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