CK Clinical are working on behalf of a top Pharmaceutical company in Belgium for a contract Biostatistician.
Tasks
Responsible for statistical aspects of clinical and pre-clinical research projects including study design, sample size estimation, patient randomisation, 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: Clinical Operations; Regulatory Affairs; Clinical Department; Clinical Pharmacology; Quality Management Profile
Masters 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 organisational skills, works towards and meets deadlines.
Ability to collaborate, build strong partnerships/relationships with all stakeholders
This is a very exciting 8 month contract with an hourly rate up to 68.45 EUR per hour (40 hours per week).
If you are interested in being put forward for this role, please get in touch with a copy of your CV to [log in to unmask] Alternatively please feel free to get in touch if you would like to hear more on 01438 768713.
Many thanks
Stephanie Maccioni
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