JISCMail - ALLSTAT Archives

Morning ALLSTAT,

I would like to introduce SRG – Scientific Recruitment Group. SRG is one of the UK’s leading specialist resourcing organisations. SRG works with world leading healthcare, fmcg and technology companies.

SENIOR/PRINCIPAL SAS PROGRAMMER

CONTRACT

CRO

SOUTH-EAST OR HOME-BASED

COMPETITIVE HOURLY RATE

Key Responsibilities

To lead/project manage studies and program Statistical Analyses and Reports
To be responsible for developing, maintaining and validating standard data structure and software
To monitor procedures for program development and validation
Interact with Client Biostatisticians, Pharmacokineticists, Medical Writers, Clinical Systems Developers, and other Operations staff
Understand and have awareness of project budgets for Clinical and Statistical Programming tasks and communicate potential issues to the Project Lead and/or Functional Manager
Create specification documents for handling and programming the clinical data, including data conversion and derived dataset specifications
Develop and/or re-use SAS programs to provide input into the Statistical Analysis Plan and creation of Tables, Figures, and Listings specifications, collaborating with the Lead Biostatistician in order to provide high quality Statistical Analyses
Expertise in the use of SAS (Macros, SQL, efficient Programming) and other in-house reporting systems
Strong understanding of the regulatory process and detailed understanding of the analysis, reporting process and implications for Clinical and Statistical Programming
Ensure analysis data and programming code meet regulatory and Client standards and are consistently structured to permit efficient programming and reporting

Minimum Requirements

BSc/MSc or scientific discipline or equivalent
Minimum 6-years industry experience
Will also have an advanced and expert knowledge of SAS Programming, gained in a Pharmaceutical or Clinical Research environment and preferably have experience in using MACRO and GRAPH
An advanced understanding and experience of implementation of CDISC (SDTM & ADaM) is essential
Knowledge of different phases and types of clinical trial reporting (e.g Phase I-IV, Clinical Study Reporting, ISS/ISE including e-sub activities)
Excellent understanding of the goals of reporting clinical data
Demonstrated ability to manage own and other people’s workloads
Have expert knowledge and expertise of environments and systems used, e.g. UNIX

Please get in touch for a confidential conversation please contact me - [log in to unmask]

+44 (0) 1753 589688

+44 (0) 7880 051284

Kind regards,

Laura

+ Laura Christie
+ Biometrics Resource Manager

+ Mobile: 07880 051284

+ DD: 01753 589688
+ Email: [log in to unmask]
+ www.srg.co.uk
+ Buckland House, Waterside Drive, Langley Business Park, Slough, SL3 6EZ

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Impellam Group plc is registered in England with registered number 06511961. The registered office of Impellam Group plc is 800 The Boulevard, Capability Green, Luton LU1 3BA.

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