Clinical Biostatistician
Function
- Provide input to protocol development/sample size calculation & protocol/CRF review
- Prepare randomization schema
- Develop analysis plans
- Perform data review & statistical analyses
- Co-ordinate and produce tables, listings & figures
- Perform independent QC
- Write statistical sections for integrated reports
- Advise DM with respect to database design, validation checks & key data
- Maintain professional statistical standards
- Maintain & archive program documentation - both electronic & paper - in an appropriate manner
- Understand regulatory statistical guidelines/developments
- Project Responsibility & Customer Interaction
- Attend customer meetings to discuss project requirements/progress
- Perform Statistical Team Leader role for single study projects
Profile
- Master's degree or educational equivalent in biostatistics or related field and 3 to 5 years relevant experience
- Familiarity with moderately complex statistical methods that apply to Phase I-IV clinical trials
- Strong working knowledge of SAS computing package, CDISC Standards, familiarity with other statistical computing packages
- Pharmaceutical, drug development, biotech or CRO industry experience
- Strong written and oral communication skills in English, strong attention and accuracy with details, strong initiative, organization skills and multi-tasking ability, ability to lead and co-ordinate small teams
Location
Woluwe-Saint-Lambert
Contact person
Baltazar