Dear Allstat,
Please find below the details for our latest contract position based in
Germany.
This position is 12 months initially with our client ideally looking for
candidates to stay for the long term.
The rates are dependent on experienece but you can typically expect around
€70/hr.
Background information:
The candidate will work in our Phase I/IIa biostatistics team (5
Statisticians) and be responsible for planning and analysing Clinical
Pharmacology studies.
Typical study types are Bioequivalence , Bioavailability (Drug drug
Interaction, Drug Food Interaction, Drug Formulation BA studies), Single
Rising Dose, Multiple Rising Dose etc.
Scope of work:
The candidate will act as a fully responsible trial statistician.
He/she will collaborate with the Clinical Pharmacologist, Clinical
Kineticist, Data Manager and SAS Programmer.
For non-complex trials, the analysis and reporting may be contracted out to
specialized CROs, while for complex trials, analysis and reporting is done
inhouse involving SAS Programmers to execute the Trial Statistical Analysis
Plan (TSAP).
For report writing, a medical writer is also involved.
As usual in Phase 1, standard specifications (TSAP, tables, graphs &
listings) and analysis tools (SAS macros for BA/BE/dose proportionality) are
available to handle routine tasks efficiently.
Qualification:
MSc or PhD in statistics or math. Experience working as a statistician in on
Clinical Pharmacology studies a Pharma company / CRO. Excellent general
biostatistics knowledge. Good knowledge about pharmacology and kinetics.
Good communication skills.
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