Dear all,
Great opportunity has arisen for an experienced Statistician to join one of the leading pharmaceutical companies located near London.
Responsibilities:
The Senior Statistician is responsible for the biostatistical aspects of Clinical Development projects.
On project level this includes development of strategies for clinical development plan with clinical team and interaction with clinical/statistical experts.
On study level this includes protocol contributions, case report form definition, scheduling of analyses using the Data Reporting Analysis Manual to help maintaining consistency across the project and finally conducting analyses to providing objective interpretation of results and defense of statistical decisions to clinical team, DST, Life Cycle Team and regulatory health authorities.
He/She organizes the workflow and plans and monitors resources.
Requirements:
MSc (or equivalent) or PhD in Statistics or very similar area
Substantial pharmaceutical industry experience in Biostatistics and clinical drug development
Directly relevant oncology experience to enable you to lead Biostatistics activities on Phase 3 studies, including both internal and external meetings
Ability to process information, analyse data, and reach conclusions based on sound reasoning
Ability to work in a global team, frequently in a matrix manner
Experience in using statistical software (particularly SAS, R or S-Plus).
Very good English language skills
This role is offering a very competitive salary package for the right candidate.
If you have the skills and experience for this opportunity please email your C.V. to [log in to unmask] or call +441273 727 930 for further details.
Andrea is a Clinical Operations Search/ Biometrics expert at Stelfox Pharmaceutical Search covering Europe, UK, North America and Asia.
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