Dear Allstaters,
please find below the latest contract vacancy for you to review;
Essential; educated to at least MSc. in statistics / biostatistics / related
subject, 5 years statistics experience within a clinical trials environment,
excellent clinical trials methodology / analysis planning / reporting of
early clinical trials / statistical analysis, ability to lead statistical
aspects of a clinical trial, strong SAS programming, SAS/base, SAS/macro,
SAS/graph & PROC/Report. Desirable; ODS or experience of early clinical
development including statistical analysis of pharmacokinetic data.
Working for this major pharmaceutical client you will be reporting to the
group head of statistical reporting, duties will include;
- Responsible for all statistical tasks of the assigned Early Clinical
Development (ECD) trials (including specification of analysis plans,
statistical consultation during the running phase plus writing statistical
sections of clinical study reports).
- Responsible for reporting and statistical analysis of safety,
pharmacokinetic and PD data from individual studies
- Track clinical trial/allocated project activities and milestones.
- Subsequent timely delivery of high quality tables, listings, graphs and
statistical analysis of clinical trials and project deliverables from
analysis plan, including ad-hoc exploratory analyses
- Represent line function within clinical teams
- Ensure that documents and specifications are consistent and comply with
company standards
LOCATION: Switzerland
START DATE: ASAP, but they will wait for notice
If you are interested in this position please contact me for a further brief
discussion about the role...
James Carrera
European Contracts Manager
Pharmaceutical, Healthcare & CRO division
1st Pharma People
"A Division of 1st IT People"
Tel: +44 (0) 207 255 6665
Mobile: +44 7717 578 246
Fax: +44 (0) 207 255 6656
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