Dear ALLSTAT, please see below details of our latest opportunity
Senior Statistician - Permanent role - Office based, South East – UK
An exciting opportunity for a Senior Statistician to join an international CRO specialising in Biometrics to join their rapidly expanding team.
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Responsibilities and required experience
• Provide statistical consultancy on the protocol design including sample size calculation.
• Collaborate with the clinical trial team in preparing the eCRF and either review or prepare the Validation and Analysis Plan modules (eg. edit checks, protocol violations, etc.).
• Review of data transfer specifications.
• Provide input on the statistical methodology, review the statistical analysis plans and summarize comments/mistakes. Drive the finalization of the documents according to the standards.
• Review programming specifications.
• Review the draft statistical outputs and final statistical analysis results and help the medical team with the interpretation of data.
• Provide support in planning and organizing Data Monitoring Committee (DMC) meetings
• Support/review the preparation of abstracts/posters/manuscripts/DMC reports as well as clinical study reports.
• Perform ad-hoc statistical analyses, if needed. All outputs, including SAS programs used to generate the outputs, should be made available.
• Attend to ad hoc face to face meetings/TCs with Regional Medical Manager/Directors, as needed.
All services should be delivered according to the client’s procedures & standards and timelines that will be agreed time to time.
Oral and written English is mandatory.
Some initial training related to the use of company tools and templates will be provided at the beginning.
For further information, please contact me directly at [log in to unmask]
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