Senior Statistician - Phase III
Mainland Europe
6 month Rolling contract - Excellent rate / hour
We are currently looking for an experienced Statistician to support late stage clinical trials.
Main responsibilities include:
- Preparation of statistical analysis plans.
- Perform statistical analyses in SAS and collaborate with the statistical Programming team to preparing SAS programs for analysis and reporting.
- Interpretation of study results
- Writing of clinical study reports and scientific publications.
- Provide statistical input to medical monitoring activities.
You will have;
At least 5 years of relevant biostatistical experience in late stage clinical trials including, but not limited to, the conduct of efficacy and safety analyses of phase III clinical trials.
* Expert in the analysis of mixed models, including repeated measures analysis and survival analysis.
* In-depth knowledge of clinical trial design (sample size, superiority/equivalence/non-inferiority, multiplicity, etc.).
* Excellent scientific writing skills.
* Good knowledge of SAS programming, SAS/base, SAS/macro, SAS/stat & SAS/graph.
Regards
For immediate consideration please forward your CV to [log in to unmask] or call...
James Carrera
Manager - Pharmaceutical Division
SEC Pharma
0044 (0) 207 225 6665
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