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We have a great permanent role for an Expert in Clinical Trials
Methodology.

The role will be working globally to lead and consult with teams in
innovative clinical trial design from the statistical perspective.

Ideally, you will have research and methodological experience and be
published in the following areas:

   - advanced/adaptive clinical trial design
   - multiplicity
   - subgroups and biomarkers
   - decision analytics

Experience:

   - High level of competence in global and cross-skilled collaborative
   working in statistical teams
   - Application of expertise on practical problems, for the benefit of
   patients, with proven examples
   - PhD in Statistics, followed by strong experience of independent
   academic research and/or clinical drug development
   - Knowledge / research experience in group-sequential/adaptive designs,
   multiple testing, Bayesian statistics, optimal design theory, missing data,
   non-linear and mixed effect models
   - Ability to implement methods computationally in the candidate’s area
   of expertise, in for example R, SAS (or other language)
   - Broad awareness of statistical issues against the evolving scientific,
   regulatory and payer arenas

This is a key role and therefore has a great salary and benefits package
associated with it.

Please let me know if you are interested in discussing this further with me
or directly with our client.

Gail

Managing Director

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