FREELANCE: SAS Programmer - Diabetes / CDISC
Mainland Europe 6-12 month contract
Accountabilities/Responsibilities:
The candidate will join a team and be involved in:
*Extracting safety and non-safety data into Client's in-house reporting system using a standard interface.
*Writing and validating software according to statistical analysis plans and Client programming standards.
*Using a pre-defined checklist to assess quality of safety outputs, and creating a checklist to assess quality of other outputs.
*Producing pre-defined safety tables, listings, figures, datasets, and some non-safety tables by running software within the reporting system.
*Ensuring the high quality of all outputs by examination according to a checklist.
*Identifying the general cause of any reporting issues (e.g. data or programs) and their possible resolution with data management and/or programming staff as appropriate.
*Becoming familiar with the safety and non-safety profile of a research drug and being able to discuss this with other project members.
Training will be given in all Client specific tools and processes.
Essential Skills & Capabilities:
5 years+ Statistical Programming experience within the pharmaceutical industry
Preference will be given to candidates who meet the following criteria:
5+ years of SAS/Stat
Knowledge and experience of SAS/Graph
Knowledge and experience of SAS/SQL
For further details or a confidential conversation please contact me directly:
James Carrera
Manager - Statistics, Biostatistics & Programming
Pharmaceutical, Healthcare & CRO Division
SEC Recruitment
Tel: +44 (0) 207 255 6665
james.carrera@secpharma.com
http://uk.linkedin.com/in/jamescarrera
Pharmaceutical, clinical trials, statistician, statistics, statistical, SAS, programmer, programming, statistics, statistician, biostatistics, biostatistician