Dear Allstat,
Please see below details of our latest opportunity to work for a major pharmaceutical company based in Denmark. Contract positions.
This is an urgent project. Candidates will be required on site initially for 2-3 months and after this time 50 % on site and 50 % home based work anywhere in Europe is an available option.
The ideal candidate’s will be experienced Statistician’s with at least 2+ years knowledge and experience of the clinical research industry. The candidate’s will be responsible for the design, analysis and reporting of clinical trials and must have good SAS programming skills.
Responsibilities,
The design, statistical analysis and reporting of individual studies. Developing statistical analysis plans and statistical reports. Provide quality control checks on tables, figures and listings.
Experience, Skills, Knowledge
-Excellent understanding of the drug development industry
-Good knowledge of clinical trials within Pharmaceutical environment
-Strong statistical analysis background/experience
-Fundamentals of project planning and management
-Strong knowledge of commonly-used statistical concepts, practices and procedures
-Clear and effective communication of statistical information (written and oral)
-Strong statistical programming skills using SAS.
Education/Qualifications
• MS/MSc or Bachelors equivalent in Statistics, Biostatistics, Mathematics or other subject with high statistical content
• Good knowledge of English in a business environment
For further details, please contact me directly at [log in to unmask]
Kind regards,
Rachel Keay
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