Morning Allstat
SRG Clinical have two permanent Statistical Programming roles with an
established pharmaceutical company in France. One position is for a
candidate with significant industry experience (CRO, pharma or biotech)
within a statistical programming role and the other can be a little less
experienced as there is room within the team to offer growth & support.
In both roles, you are a member of the Clinical Trial Team and
responsible for all implementation in SAS of any outputs of the clinical
reports. You will collaborate closely with the project programmer to
implement template program and will follow the Good Programming Practice
and a harmonized programming approach across trials. You will:
* participate in the blinded report planning meeting
* be co-responsible with the Statistician for the specification for the
analysis dataset plan
* together with the Statistician, be responsible for the Mock Report SAS
implementation, including the analysis datasets, tables, graphs and
listings
* implement outputs from the Medical Quality Review Meeting according to
specification providing from the Trial Statistician
* in case of outsourcing of the validation process, you will be the
contact person for the validation of the analysis datasets
You will have excellent experience in SAS V9 and experience in Clinical
report SAS implementation. You must be eligible to work in the EEA and
have excellent written and spoken English. French language skills are an
advantage.
For more information please call Helena on +44 207 562 1792 or email
your CV to [log in to unmask] <mailto:[log in to unmask]>
best wishes
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/>
Please note I work Monday - Thursday
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