Good Morning Allstat,
SEC Pharma is currently recruiting for a Contract SAS Programmer to work on an initial 6 months basis, with a clinical trials organisation based in London with some flexibility
to work from home.
Key Responsibilities: Programming includes, but is not limited to the data manipulation, analysis and reporting of primarily clinical trial data. Specifically, analysis files
creation; table/listing/graph generation; program validation and documentation; and output verification. Work is to be performed in a team environment, where team members may be distributed across locations.
Basic Qualifications:
Proven leadership skills and/or advanced technical skills, a greater understanding of industry and regulatory standards and processes (filings, CDISC SDTM and ADaM)
•Ability to work, communicate and take direction from a globally dispersed virtual team
•BA/BSc or higher degree in Computer Science, Statistics, Mathematics, Life Sciences or other related scientific subject, or work experience equivalent
•Specialist relevant programming experience in a clinical development environment
•Excellent SAS data manipulation, analysis and reporting skills
•Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials data
•Ability to work effectively and successfully in a team environment
•Excellent oral and written communication skills
•Ability to provide quality output and deliverables, in adherence with challenging timelines
•Willingness and ability to learn and follow standard processes and procedures.
Key Criteria:
1) SAS experience within a Clinical Trial setting (SAS v9.2+ Modules Base, Stat, Graph, Macro, Enterprise Guide, SQL) preferably within a high profile Pharma Company in Europe
2) Relevant BSc (Stats, Computer Science, Maths, Information Systems, Operational Research)
3) Working with CDISC Standards (SDTM and ADaM) + formal training preferred
4) Producing Tables, Listings and Figures
5) Some leadership experience (either lead Programmer or responsible for delivering a series of studies)
6) Involved in global initiatives (developing standards, process or technical enhancements)
For immediate consideration, please contact Priya Mukherjee on: +44(0)207 255 6665 or email an updated CV to
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Best wishes,
Priya
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