For a confidential consultation call James Carrera on 0044 (0) 207 255 6665 or email your CV to
[log in to unmask]
0301/12c
CONTRACT: Senior Statistical SAS Programmer
Statistical Reporting
within Health Outcomes
12 months rolling contract
Job Summary:
For this major pharmaceutical client you will work with Health Outcomes specialists (Patient Reported Outcomes
Specialist, Epidemiologist, Health Economist) and programmers based also in other sites. Primarily providing programming support to Healthcare Outcomes and the Pharmaco-Epidemiology team.
Accountabilities/Responsibilities:
·
Provide programming support and validation of analysis data sets, pooled datasets, statistical summary tables, figures and patient data listings for
phase I – III clinical trials, ISS & ISE, primarily using SAS.
·
Provide output for the Clinical Study Report, the Integrated Summary of Safety (ISS), the Integrated Summary of Efficacy (ISE), electronic submissions
and Exploratory Health Outcomes Research Reports.
·
This position will require a significant training investment for the use of client technology in relation to SAS macros, creation of analysis data
sets and dataset structures. Need for ensuring standardization of programs where applicable.
·
Apply knowledge of clinical data, the design and phases of clinical trials, statistics, relevant regulations and the pharmaceutical industry to the
implementation of tasks.
·
Handle complex statistical programming issues independently and be familiar with study programming issues. Bring ideas for new projects and take the
initiative to solve issues.
Essential Skills & Capabilities:
At least 5 years Statistical SAS programming experience with prior experience in pharmaceutical related field
is required (experience with large databases is an asset).
Working knowledge of clinical legislation (FDA, EMEA, ...), Good Clinical Practice (GCP) and Clinical Data
Interchange Standards Consortium (CDISC) is a plus.
·
SAS expert
·
Statistical knowledge including basic statistics (descriptive statistics, inferential parametric and non parametric analyses) and advanced statistical
techniques (multivariate analysis, ...).
·
Fluent in English
·
Ability to understand business problems rapidly and to reformulate them in terms of appropriate statistical analyses to be performed.
·
Ability to evaluate processes and situations in an orderly and rational manner asking questions and identifying missing information.
·
Accurately and efficiently work towards quality results
For further details or a confidential conversation please contact me directly:
James Carrera
Manager - Statistics, Biostatistics & Programming
Pharmaceutical Division
SEC Recruitment
Statistics, Biostatistics & Programming
Tel: +44 (0) 207 255 6665
[log in to unmask]
http://uk.linkedin.com/in/jamescarrera
Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician