Clinical Statistician (m/F)

mardi 24 juillet 2018
Date limite
vendredi 24 août 2018
Andrea Baetens
Niveau d'expérience
5 à 10 ans d'expérience
Type de contrat
Temps de travail
Temps plein
eXPErt services for eXPErt professionals.
That's XPE. For one of our clients we are looking for: Clinical Statistician (m/F) Organisation description:

Within the Biostatistics & Data Management team, biostatisticians provide statistical expertise and support in the development of prophylactic or therapeutic vaccines. We are currently looking for consultant biostatisticians in epidemiology. You will join a team of about 75 statisticians that are devoted to the discovery and development of vaccines.

Job description:

As biostatistician, you will: be responsible for the statistical designs of epidemiological studies, creating statistical sections for study synopses and protocols input in study set up (case report forms, database, e-diary, data management plan, etc.) propose and evaluate the performance of statistical methods in order to prepare statistical analysis plans write and execute SAS programs to analyze the data and to report results in tables, listings and figures perform statistical analysis, run simulations and discuss with internal and external experts support scientific writers and clinicians to correctly interpret the statistical results and align them with the clinical report conclusions write the statistical sections of clinical study reports, statistical publications and prepare materials for publications and create statistical text for clinical study communications


You have: M.Sc. or Ph.D. degree in Biostatistics or Epidemiology (or equivalent) At least 2 years of experience as biostatistician in the Pharmaceutical/Epidemiological field Knowledge in epidemiology Comprehensive understanding of applied statistical principles and modeling in the design and analysis of epidemiological studies. Experience in statistical methodology research and presentations on statistical methods, observational study design, and analysis in either observational studies or randomized studies. Proficiency in SAS (knowledge of other statistical software is an asset) Good skill in written and spoken English Ability to easily communicate with different functions: clinicians, scientists, data managers, scientific writers, commercials, etc. in an international, multi-cultural environment Compliance with internal Standard Operating Procedures and regulatory guidelines


We offer you a permanent contract with XPE Pharma as Consultant, a job in a Great place to work

XPE Personnel Services NV/SA: Flanders: VG15/BU, Brussels: B-AA5.031, Wallonia: W.RS.002/W.INT.002
XPE Group NV/SA : Flanders: VG1834/B, Brussels: B-AA11.007, Wallonia: W.RS.713

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