Statistician, SAS programmer and RWE Data Analyst with over 20 years’ experience in the pharmaceutical industry

Functioned as a clinical trial statistician, project statistician, Interim SAS programming lead and RWE Analyst

Excellent communication skills have been developed through leading teams of statisticians and programmers and providing statistical support on clinical and RWE projects and through substantial liaison with internal and external customers

RWE Statistician using Marketscan, CPRD, AURUM, Maccabi, Optum, many other claims & EHR databases

Collaborating with medical affairs, HEOR and market access functions to help develop client's portfolio in the post approval space

Main indications are Neurology, Respiratory, Immunology

Working as data analyst/SAS programmer in RWE (Real World Evidence) group

Programmatic and statistical review of epidemiologybased analysis plans and protocols

Causality methods, propensity score matching, IPTW

Developing SAS tools for use in the extraction and preparation of data for analysis

Extensive use of the CPRD DEFINE and EXTRACT online tools

Designing and implementing reports in SAS (BASE, STAT, MACRO, ODS GRAPHICS, PROC SQL)

Databases include CPRD GOLD, AURUM, HES, ONS Death, IMD and IBM MARKETSCAN

Indications: Neurology, Immunology

Trial Statistician for three phase III pivotal trials

Protocol design, specification of the primary analysis variable and secondary analysis variables, detailing hypotheses to be tested in terms of population parameters, specification of analyses methods

Write statistical analysis plans to document in detail how the planned analysis will be implemented. Produce table, figure and listing (TFL) shells

Design analysis datasets (CDISC, SDTM, ADAM Data conventions), working with study programmers to design the datasets needed to implement the planned analyses

Blinded review meeting to define analysis populations (ITT, Per-Protocol, Safety)

Validation of key analysis datasets through double programming

Review of all outputs produced by the programming group

Liaise with medical writing team to support the production of the clinical study reports

Indications: Epilepsy, RA, CD