SEC Recruitment Ltd - Senior Biostatistician
| Employment Type: | Permanent |
| Location: | Brussels, Belgium |
| Salary: | |
| Languages: | English |
Our client is an international pharmaceutical company located in Belgium and currently seeking a Senior Biostatistician to join their team located in Brussels area. For more information, please contact Louise Beka.
As a Senior Biostatistician, your main responsibilities will be as follow:
• Provide statistical providing statistical input to projects in Clinical Development
• Works as the lead statistician on the projects
• Participate in the training sessions for the department
• Work on the improvement of internal statistical procedures
• Evaluate and implement improved statistical procedures
• Keep abreast of the relevant biometrics advances and recommend changes and new statistical techniques
To be considered for the position, you have the following attributes:
• MSc or PhD in statistics, biostatistics, mathematics or related discipline
• 4+years Experience in applied statistics to clinical trials
• Strong SAS knowledge and ability to program in SAS
• Fluent spoken and written English
• Knowledge of the following techniques: experimental design issues; mixed models techniques; basic data analysis methods
• Knowledge of the regulatory aspects of drug development
If you are interested in this position, please do send your CV with a cover note to Louise Beka
As a Senior Biostatistician, your main responsibilities will be as follow:
• Provide statistical providing statistical input to projects in Clinical Development
• Works as the lead statistician on the projects
• Participate in the training sessions for the department
• Work on the improvement of internal statistical procedures
• Evaluate and implement improved statistical procedures
• Keep abreast of the relevant biometrics advances and recommend changes and new statistical techniques
To be considered for the position, you have the following attributes:
• MSc or PhD in statistics, biostatistics, mathematics or related discipline
• 4+years Experience in applied statistics to clinical trials
• Strong SAS knowledge and ability to program in SAS
• Fluent spoken and written English
• Knowledge of the following techniques: experimental design issues; mixed models techniques; basic data analysis methods
• Knowledge of the regulatory aspects of drug development
If you are interested in this position, please do send your CV with a cover note to Louise Beka
You cannot apply for this job as it is no longer active.
Back to search.