Job Biostatistics
To provide statistical expertise in the design, planning, conduct, analysis and reporting of clinical studies. To ensure statistical validity and overall quality of deliverables.
Scope
Statistical support for all studies analyzed on behalf of the sponsor by 4Clinics. Will have much direct contact with the client, both the statistical and clinical teams. Will work together with Clinical Data Managers, Clinical Data Analysts and Medical Writers to produce high quality results.
Key Responsabilities
- Define methodology of the study
- Calculate sample size and writes statistical sections of the protocol
- Write the Statistical Analysis Plan
- Create counting rules to be included in the Data Dictionary Table (DDT)
- Perform quality control of analysis datasets
- Develop and maintain statistical programs as necessary to perform analyses, to prepare data displays and to verify data accuracy
- Perform statistical analyses and interpret the results
- Write sections of CSRs or publications as needed
Qualification
- Master's Degree in Sciences preferably in Computer Science, Life Sciences or related fields with post-graduate degree in Statistics or Biostatistics.
- Must have at least 5 years clinical trial experience to write protocols
- Extensive SAS knowledge, other statistical software knowledge is a plus
- Excellent communication skills in English, both written and verbal
- Able to explain statistical concepts to non-statisticians
- Good team player and flexible to work on diverse projects in various disease areas
Place
The position can be based in Waterloo (Belgium) or Paris (France).
Apply here: http://www.jobsinbrussels.com/ads-4Clinics-Biostatistician-70602.aspx