Description
An excellent opportunity has arisen for a Senior Biostatistician to join a global Pharmaceutical company based in Belgium. This is a 12 month contract and will focus within Phase 2 & 3.
Responsibilities:
*Responsible for statistical aspects of clinical and pre-clinical research projects including study design, sample size estimation, patient randomization, case report form development, writing statistical analysis plans, statistical analysis and interpretation of data, and reporting of results.
*Work with SAS programmers as part of a biostatistics team.
*Knowledge of applied parametric and nonparametric statistics, strong SAS programming skills, and the ability to translate client needs into statistical practice and the ability to educate clients in the use of statistics are essential.
*Biostatistics, SAS programming, Clinical Data Management and Medical Writing.
*Contacts inside the company depending on level of experience
Experience Required:
*Master's Degree in Statistics or PhD in Statistics or related field.
*Basic knowledge of SAS programming and at least some other significant statistical software (e.g., S-Plus, PASS).
*Knowledge of Microsoft Office applications
*Excellent interpersonal skills, great understanding of team-culture.
*Demonstrate a nature of proactively, enthusiasm, independent drive, and energetic outlook to tasks
*Exceptional organizational skills
*Ability to collaborate, build strong partnerships/relationships with all stakeholders
For further information about this role, or to discuss other vacancies, please contact Tim Barratt on +44(0)1727 817 626 or email tbarratt@keypeople.co.uk
