We are currently seeking 3 Statistical Programmers with a minimum of 2 years' experience in SAS Statistical programming applied to clinical trials. This role will offer a great opportunity to grow within an international team and you will be trained to the latest CDISC standard.
Ref: 285 12BG
6 months (+extensions)
For a confidential consultation call Fida Larbi on +44 207 255 6665 or email your CV to [log in to unmask]
PRINCIPAL RESPONSIBILITIES:
- Co-ordinate the programming of analysis datasets, using specific SAS macros.
- Co-ordinate the creation of the metadata files (define.xml) using specific SAS macros.
- Co-ordinate the production of tables, listings & figures
- Co-ordinate the restructuring, review and integration of external data
- Co-ordinate the generation of consistency check programs and QC listings
- Co-ordinate the transfer of data according to customer specific requirements
- Develop adequately documented programs for the generation of randomisation schema/program
PROFILE:
- 2 to 5 years of relevant clinical trial SAS experience
- Proficient SAS programming skills with mastery of SAS/STAT SAS/BASE, SAS macro language. SAS/GRAPH is a nice to have
- Capacity to interface with clinicians, statisticians and data managers as statistical programmer in charge of a clinical trial
- Able to read, write and speak fluently in English.
For further details or a confidential conversation please contact me directly:
Fida Larbi
Consultant - Pharmaceutical, Healthcare & CRO Division
Statistics, Biostatistics & Programming
Tel: +44 (0) 207 255 6665
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