Background:
This role will see you join a dynamic and professional Statistical Team.
Once on board, you can expect to be developed and take on real
responsibility, both internally and externally (CRO Management).
You will be required to travel to the US and Japan to represent the
organisation and be trained appropriately.
Primary Duties:
The purpose of this position is to provide program-level statistical
programming expertise by:
Designing and executing analysis deliverables to meet the requirements
of clinical studies.
Managing and enforcing standards for derived datasets and analysis
outputs to maximize global data integratability.
Directing the work of external vendors providing statistical programming
services to achieve quality and timely, cost-effective study
deliverables.
Represent the statistical programming function in support of assigned
clinical studies and programs lead from the US or EU.
Define and manage derived data set and reporting standards
Independently develop, execute, and maintain SAS* computer programs,
including macro programs, according to Statistical Analysis Plans
(SAPs), cross-study analysis and data specifications, or analysis
requests.
Identify vendor requirements and participate in the evaluation/selection
of BDM vendors.
Provide technical oversight of statistical programming activities of
external vendors to assure timeliness and quality of analysis data and
statistical outputs.
Review and approve key statistical programming vendor deliverables.
*Full Job Description available on request.
Experience and Qualifications:
Pharmaceutical experience as a statistician / Statistical Programmer
SAS (BASE / STAT / GRAPH)
Flexible mindset with the ability to show initiative.
Contact:
Christian Simon - Resource Executive
Tel: 020 8560 2300
Send your CV quoting job ref AS3684
AXESS Limited, Parkshot House, 5 Kew Road, Richmond, Surrey. TW9 2PR
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