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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 BIOSTATISTICIAN
CONTRACT
CRO
SOUTH-EAST OR HOME-BASED
COMPETITIVE HOURLY RATE

Key Responsibilities


  *   Performs Lead Statistician activities for allocated projects
  *   Co-ordination of QC effort for allocated projects
  *   Contributing to the statistical sections of reports integrated clinical/statistical reports and manuscripts

*         Prepare statistical sections of protocols

*         To develop statistical analysis plans and SAS data sets

*         Oversee and be responsible for SAS programming, program validation and preparation of program documentation including requirements and specifications

*         Perform statistical analysis and reporting results

*         Provide consultation on experimental design, statistical methods and approaches for the purpose of assessing safety and efficacy of drug products

*         Communicate with customer and vendors on statistical questions

  *   Primary responsibility and/or accountability for the statistical analyses, tabulations, graphics and listings of clinical trial data
  *   Ensuring statistical reports meet regulatory and company standards
  *   Develop knowledge in the use of SAS (e.g. macros, statistical procedures) and other in-house reporting systems
  *   Develop knowledge in the set-up and use of the reporting environment
  *   Provide training/guidance to less experienced statisticians
  *   Thorough understanding of the regulatory environment
  *   Provide independent consultancy level expertise and statistical services to the study team


Minimum Requirements


  *   BSc/MSc or scientific discipline or equivalent
  *   Minimum 6-years industry experience
  *   Extensive hands-on Statistical experience
  *   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 skills and goals of reporting clinical data
  *   Good knowledge of SAS, SQL and Unix
  *   Prior experience of training and mentoring of others in this field
  *   Demonstrated ability to manage own and other people's workloads
  *   Broad understanding of statistical methods within the context of clinical and/or clinical pharmacology trials

Please get in touch for a confidential conversation - [log in to unmask]<mailto:[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]<mailto:[log in to unmask]>
+ www.srg.co.uk<http://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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