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Statistical Services for Clinical Trials
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Efficient work for single studies or multiple
studies, phases I ‑ IV,
health economic and post-marketing surveillance studies.
- Design, development and review of
statistical aspects of protocols
- Sample size calculations and randomisation
schemes
- CRF review
- Integrate
with client systems as required
- Statistical
analysis plans
- Statistical
programming (SAS and Excel)
- Production
of tables, figures and listings for interim and final analyses
- Generation
of randomisation codes
- Statistical
reports
- Statistical
support and review for publications and abstracts
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Statistical
Consulting
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With more than 25 years of
industry experience, I offer knowledgeable advice focused on your needs.
- Auditing statistical analysis plans
- Auditing statistical analyses
- Independent
programming verification
- Exploratory
Analysis
- Data
Monitoring Committee Support
- Representation
of clients at regulatory agencies and meetings
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Statistical
Programming
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- Base SAS (data step
programming, macro facility)
- SAS/Stat (including use
of PROCs CATMOD, FREQ, GLM, MIXED, LIFETEST,
LOGISTIC, PHREG)
- SAS/Graph (including PROCs GPLOT, GCHART, GFONT, GREPLAY, annotate
facility)
- Excel and VBA for
statistical analyses and graphical presentations
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On-site
Contract Services
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Although
I have my own premises and equipment, I can provide my services on your
premises if you wish. I have supplied on-site contracting services to
several pharmaceutical companies of varying sizes and to a number of CROs. Services provided have included statistical
management work (supervision and recruiting of staff), statistical
consulting, data management and data entry work and SAS programming.
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