Terug naar zoeken.SEC Recruitment Ltd - Senior Biostatistician - Pharma
| Arbeidstype: | Permanent |
| Plaats: | Belgium |
| Salaris: | €4500 - €5000 per month + Benefits |
| Talen: | Engels, Frans, Nederlands |
Details van de adverteerder
- Naam:SEC Recruitment Ltd
- Gepost:22-09-2010
- Code:9917SEC/STAT/BE/Pharma
Our client is an international pharmaceutical company located in Belgium. They are now looking for a Biostatistician to join their team.
As a Biostatistician you will work on the development of statistical methodologies and implement statistical analysis of the studies.
In addition, you will be responsible for the development of statistical standards for the trials. You will be in charge of writing methodology, statistical sections of the studies protocol, statistical analysis plans and you will be in charge of the statistical analyses for trials.
You will also monitor the statistical and programming activities, write the statistical analysis and the statistical part of the studies report.
In order to qualify for the role, you are an experienced Biostatistician with MSc or a PhD in Statistics/Biostatistics or equivalent. You have at least 5 years experience as a Biostatistician within a pharmaceutical/biotech company or a CRO.
In addition, you have an excellent knowledge of SAS programming for clinical trials and you are fluent in English.
An experience within an international environment is preferable and a strong knowledge of regulatory guidelines specific to the pharmaceutical industry and clinical development is required.
If you are interested in applying for this position, please contact Louise Beka on +44 207 255 66 00 or send your CV with a cover note to louise.beka@secpharma.com
As a Biostatistician you will work on the development of statistical methodologies and implement statistical analysis of the studies.
In addition, you will be responsible for the development of statistical standards for the trials. You will be in charge of writing methodology, statistical sections of the studies protocol, statistical analysis plans and you will be in charge of the statistical analyses for trials.
You will also monitor the statistical and programming activities, write the statistical analysis and the statistical part of the studies report.
In order to qualify for the role, you are an experienced Biostatistician with MSc or a PhD in Statistics/Biostatistics or equivalent. You have at least 5 years experience as a Biostatistician within a pharmaceutical/biotech company or a CRO.
In addition, you have an excellent knowledge of SAS programming for clinical trials and you are fluent in English.
An experience within an international environment is preferable and a strong knowledge of regulatory guidelines specific to the pharmaceutical industry and clinical development is required.
If you are interested in applying for this position, please contact Louise Beka on +44 207 255 66 00 or send your CV with a cover note to louise.beka@secpharma.com
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