CONTRACT: Senior Statistician
12 month rolling contract - Mainland Europe OR UK based
Job Summary:
My client are a genomics-based pharmaceutical company dedicated to improving
the lives of patients by developing novel pharmaceutical products that
address unmet medical needs.
Accountabilities/Responsibilities:
* Working with Clinical and Biometrics Groups, write Statistical
Section and Statistical Analysis Plans for clinical trials.
* Review and provide input to statistical plans written by others.
* Review relevant clinical literature to perform power calculations to
support the number of patients to include in a clinical study.
* Review Case Report Forms (CRFs) to ensure all relevant data
necessary for data analysis is captured.
* Select appropriate best-practices randomization and stratification
schemes for study design.
* Provide, as needed, designs for interim analyses with knowledge of
FDA and EMEA guidelines for study size and power calculation adjustments.
* Analyze clinical study data using SAS (Windows-based) and provide
written reports of results.
* Review study reports provided by CROs.
* Provide additional support, as needed, for PreClinical data
analysis.
* Must be able to work both independently and as an effective team
player within the Biometrics Group and across disciplines with the Clinical
and PreClinical Groups.
* Excellent written and verbal communication skills are required.
* Experience with experimental design, general linear models, survival
analysis, analysis of repeated measures, multivariate data analysis,
permutation tests and multiple testing adjustments are necessary.
* Programming experience in SAS and R (or S-Plus) is required.
* Experience with Microarray gene expression analysis and
normalization techniques is useful.
* Experience working in a UNIX environment is desirable.
Essential Skills & Capabilities:
Ph.D. in Biostatistics or Statistics and 3 years of Clinical Pharmaceutical
Industry Experience, or M.S. with a minimum of 5 years Clinical
Pharmaceutical Industry Experience.
An excellent opportunity awaits for this renewable contract. Interview times
booked and full job specification to review...
If you would to discuss this role in greater detail or your application /
suitability to this or further roles, please call me or email me in
confidence. If you are not available or suited to this position, please feel
free to pass my details on.
We also have a broad variety of other Biometric specific vacancies available
in the UK and throughout Europe. Inclusive of SAS programming, Statistical,
Clinical programming, Data Management functions, Regulatory Affairs,
Clinical Research, QA, Compliance & Validation.
For a confidential consultation call James Carrera on 0044 (0) 207 255 6665
or email your CV to [log in to unmask]
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
mailto:[log in to unmask]
www.1st-pharmapeople.com
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