Good Morning AllStat, 

Please see below a brief list of Hays Life Sciences current contract SAS
programming opportunities, these are all based in the UK for Global pharma’s
and CRO’s. 

I am not able to list all current opportunities but if you are looking
within the Biometrics field please feel free to contact me for a
confidential consultation on +44 (0) 207 633 4824 or [log in to unmask] 

1.) Global pharma – Long term rolling contract – part time home based –
South East 

Our Client is a world leading Pharmaceutical company whom are looking for
experienced SAS Programmers to join their contracting team in the UK. This
opportunity is a long term rolling contract and successful candidates would
be expected to work on TFL’s through numerous therapeutic areas.Potential
part time home working would be allowed after an initial bedding in period. 
 
Summary  
 
•Provide advice and support to the statistical team on programming
activities related to analysis and reporting of assigned drug development
study/project results. Assess and clarify requirements, provide statistical
programming solutions and ensure their efficient implementation. 
•Contribute to CRF development and data structures definitions for clinical
trials. Ensure consistency and adherence to available standards.
•Ensure that user acceptance testing on the structure and quality of data
provided by Data Management is performed. 
•Develop programming specifications and ensure consistency with the
statistical specifications for analysis datasets and TFL’s
•Plan and perform programming, validation and documentation activities for
datasets and TFL’s according to specifications, with high quality and within
agreed time lines.
•Ensure adherence to statistical programming standards, effective use of
available standard programs and compliance with Standard Operating
Procedures.
•Support regulatory submission specific activities, e.g. electronic
submission creation.
•Maintain efficient interfaces with internal and external customers.
 
Education/Qualifications
 
•University education (BSc or MSc) or equivalent in Statistics, Mathematics
or other analytical field.
•Strong knowledge of SAS programming language with SAS/Base, SAS Macro,
SAS/Graph, 
•Good knowledge of English in a business environment
•Experience within a Clinical/Pharmaceutical environment


2.) Global CRO – 6 month contract – Full time home working – CDISC SDTM

Our Client, a Global CRO are looking for an experienced SAS Programmer to
join their highly skilled team in the South East area. The contract is
initially 6 months and experience in creating datasets to SDTM will be
required. The right candidate will gain excellent hands on experience and
within CDISC (a increasingly influential standard) and a competitive
contractor rate. 

Role Responsibility 

You will plan, develop and validate project/study level programs. You will
design and develop standard project/department macro programs and data
structures. You will also be heavily involved in creating and developing
datasets to SDTM.

Additional Responsibilities:
•Project/Study Analyses 
•Responsible for the planning, development and execution of project/study
level programs 
•Maintenance of documentation and files according to departmental policy 
•Must ensure the accuracy of all project/study level output. 
•Liaison with Clients on specifications and with Data Management on database
creation, edit check specifications, data quality and query resolution.  
•Develops, maintains and validates standard data structure and software. 
•Designs and writes standard departmental macros that are maintainable,
supportable, well-documented programs that are user friendly and accessible. 
•Monitors procedures for program development and validation. 
•Technical Support 
•Assists in the training of statisticians and programmers and ensures the
development of data analysis skills.  

3.) Global Pharma – 11 month rolling contract – Full time on site – Stats
experience preferable 

Our client, a global Pharma, are looking for an experienced statistical
programmer to join their team in the UK. This opportunity will involve
leasing heavily with your European counterparts whilst also working closely
with the on-site statisticians and because of this working experience within
stats is preferable. 

Description

Provides technical expertise to execute multi-disciplinary or cross
functional projects in support of EU Statistics. Applying expertise across
therapeutic areas and phases of clinical development 

Key Objectives/deliverables 

The job tasks listed below outline the scope of the position. The
application of these tasks may vary, based upon current business needs. 

Knowledge and Expertise 

• Ability to apply innovative programming techniques to solve critical
problems 
• Collaborates with project statistician to suggest appropriate methodology 
• Develop approaches or solutions that save time, increase efficiency or
otherwise directly impact business 
• Operate in collaboration with study personnel to provide input on analysis
for the conduct of each study. 
• Assist in developing efficient working relationships and practice with TPO
partners 
• Assist in or be accountable for selecting statistical methods for data
analysis, 
• Participate in peer-review work products from other statistical
colleagues, and advise others on technical aspects. 

I am not able to list all current opportunities but if you are looking
within the Biometrics field please feel free to contact me for a
confidential consultation on +44 (0) 207 633 4824 or [log in to unmask] 


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