Job Reference: 1609-9
Job Duration:
Start date: 01.10.2016
Description:
An excellent opportunity has arisen for a Senior Statistician to join a leading Pharmaceutical company based in Paris. This role has become available due to a period of growth within the company and will offer exposure to extensive clinical development exposure within oncology and in inflammatory and neurodegenerative diseases.
Responsibilities:
*Write and review protocols
*Provide statistical analysis of clinical trial: write thestatistical analysis plan, program statistical analyzes with SAS and perform quality control of the clinical report
*Organizethe committee review the data before the base gel and the un-blinding
*Participate in discussions with health authorities (ANSM, EMA, FDA) for drafting the protocol to the registration dossier
*Validate the development and monitoring of randomization tools (IVRS and IWRS), to form project teams and users
Experience Required:
*Engineering degree with Honors in Statistics (Master 2, ENSAI ISUP ...)
*At least 5 years' of experience in the field of statistics applied in medical research (pharmaceutical, CRO ...)
*Expertise in SAS
*Strong MS Windows experience; Capture System of knowledge is a plus
*Strong English language skills
*Knowledge of international standards for statistical analysis (ICH)
For further details about this role, please contact Tim Barratt on +44(0)1727 817 626 or email a copy of your CV to tbarratt@keypeople.co.uk
Industry: Pharmaceuticals
Salary: €50000 - €70000 per annum
Salary Benefits:
Vacancy Type: Permanent
Job Skills: statistics, SAS, statistician, biostatistician, paris, france
Contact Name: Tim Barratt
Website: -
Direct Application URL: -