This job has been posted for more than 30 working days and has expired.
For a confidential discussion Russell Gillam on 0044 (0) 207 255 6665 or email your CV to russell.gillam@secpharma.com
Job Summary:
Working for the major International Company on their long term projects you will provide programming support and validation of analysis data sets, pooled datasets, statistical summary tables, figures and patient data listings for phase II - III clinical trials, ISS & ISE, primarily using SAS.
IMMEDIATE CONSIDERATION
Global Pharmaceutical
South Germany
2 X Clinical SAS Programmers
12 Months Rolling Contract
70 EURO P/H
For immediate consideration please send your CV to russell.gillam@secpharmaceutical.com OR alternatively call me on +44 (0) 207 255 6665 for a confidential consultation.
Your Accountabilities/Responsibilities:
-Provide output for the Clinical Study Report, the Integrated Summary of Safety (ISS), the Integrated Summary of Efficacy (ISE) and electronic Submissions.
-You will work with biostatisticians and programmers based also in other sites globally.
-This position will require a significant training investment for the use of client specific processes / procedures in particular, 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.
Your Essential Skills & Capabilities:
At least 4 years Statistical SAS programming experience with prior experience in PHARMACEUTICAL (CRO/biotech/pharma) related field is required.
Working knowledge of clinical legislation (FDA, EMEA), Good Clinical
Practice (GCP) and Clinical Data Interchange Standards Consortium (CDISC).
SAS expert
Fluent in English
Ability to evaluate processes and situations in an orderly and rational manner.
The ability to identify missing information.
Must be able to determine relationships between different parts of a problem and identify appropriate solutions.
Accurately and efficiently work towards quality results
An excellent opportunity awaits for this renewable contract.
To find out more details, please feel free to get in touch with Russell Gillam on +44 255 6665 OR send your CV to Russell.gillam@secpharma.com
Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician