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Job: Biostatistician x 2
Type: Contract 
Duration: 6 months ++
Location: Switzerland
 
Rolling contract opportunity in Switzerland, with a clinical trials
company, where you will be responsible for all biostatistical aspects of
the study, inform and suggest solutions to the project statistician on
critical issues within trial. 
In this role, you will ensure that the statistical part of the protocol,
the statistical analysis plan and the study reports are reviewed and
approved by the project statistician and discuss protocol and CRF and
data transfer specifications with the authors. 
You will write the statistical section of the protocol stating the
hypothesis, defining the planned analysis, primary and secondary
variables, time periods, interim analysis specifications,
intent-to-treat population and explaining the statistical basis for the
choice of sample size. 

Your other responsibilities include:
Planning details of the randomization schedule, approving the
randomisation list, verifying the consistency of the protocol with the
CRF/data transfer specifications, ensuring that the trial design is
compatible with the trial objective, reviews and approves protocol and
CRF/data transfer specifications prior to their use or submission to
approval committees. 
 
Educational background and experience: 
MSc in Medical Statistics or equivalent and several years experience
working in a CRO, pharmaceutical or biotechnology company. Must be
eligible to work in the EEA and have excellent written and spoken
English.
 
For a confidential discussion about this role or other opportunities
within Biostatistics with SRG Clinical please call Helena on +44 (0)207
562 1792 or email [log in to unmask]
 
All the best 
Helena
 
 
 
Helena Newman-Mitchell 
Biometrics Lead
 
Direct:    +44 (0) 207 562 1792
Fax:        +44 (0) 207 562 1799
Mobile:   +44 (0) 782 536 2548
Email:     [log in to unmask]
Website: www.srgclinical.com <http://www.srgclinical.com/> 
 
 
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