Job Details
Our client is a world leading independent biotechnology company and they are currently seeking a Contract Statistician for their offices based in the South East of England on a 6 month contract role.
JOB ROLE:
Responsible for ensuring all statistical aspects of documentation pertaining to individual clinical studies meet required standards and are statistically correct and adhering to all company policies, SOPs and other controlled documents.
PRINCIPAL RESPONSIBILITIES include:
* Coordinating the design, statistical analysis and reporting of individual studies
* Providing statistical input for publications, presentations and in-house decision-making
* Manage all study team activities within Biostatistics according to agreed resource and timeline plans
* Review and approve randomization specifications
* Create statistical analysis plans
* Write, test, validate and execute software programs to produce SDF datasets and tables, listings and graphs for inclusion within CSRs, ISS/ISE, IBs, INDs, publications and other communications
* Participate in the finalization of protocol deviations and analysis sets
* Contribute to the continuous improvement of Global Biostatistics
QUALIFICATIONS, KNOWLEDGE & EXPERIENCE:
* MS/MSc or PhD/equivalent in Statistics or other subject with high statistical content
* Statistical Analysis
* Clinical Trials within Pharmaceutical/Biotechnology/Public Health setting in Industry, Government or Academia
* Ideally Oncology experience
* Team player
Fforde is acting as a recruitment agency/business.
KEY WORDS:
Statistician, Statistics, Biostatistician, Biotechnology, Drug Development, Clinical Trials, Clinical Development, Biostatistics, Contract, England, South East
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