Principal / Senior Programmer Analyst
Harlow
Requisition no. 30625
You will be a graduate with an honours degree or MSc in statistics,
computer science, or a related scientific or numerate subject, with a
minimum of 5 years relevant experience. In addition to your excellent
written and verbal communication skills, you’ll be meticulous and have a
flair for problem solving. As an ambitious and self motivated individual,
you’ll have the ability to work effectively in a highly motivated team.
Advanced SAS® knowledge is essential
We currently have a senior vacancy within the Neurosciences area of our
Statistics and Programming Department at the New Frontiers Science Park
site in Harlow. We are looking for a Programmer/Analyst, with a minimum
of 5 years experience of SAS® programming/analysis within the
pharmaceutical, CRO or medical environment. As a key member of a dynamic
team you will be working alongside medical statisticians and other
programmer analysts and directly interacting with clinical and regulatory
customer groups.
The scope of this role will include performing and co-ordinating analysis
and reporting activities for phase II-IV clinical trials, encompassing
support work for major regulatory submission activities within the US and
EU. It may also include providing programming support for commercial
activities and regulatory agencies outside the US/EU. In addition,
reviewing protocols, Case Report Forms and Reporting and Analysis Plans,
specifying structure and content of reporting datasets, developing and
testing SAS programs and producing summary statistics in the form of
tables, listings and graphics are all activities encompassed within the
role.
The successful candidate should have proven ability to co-ordinate
reporting activities conducted by contractors based on site, and
programming personnel based at other GSK sites and/or CROs. Ability to
guide junior staff members and aid them in touble shooting are also
required attributes for this position. You should be able to work
independently and as part of a cross functional team, ensure appropriate
quality control and validation of work to meet regulatory requirements.
Please note that shortlisting preference will be given to applications
received before 23rd June 2006. Please use the "cover letter" of your
online application to describe how you feel you meet the requirements of
the role (however you are also welcome to include other information such
as salary expectations, dates you may be unavailable to interview, etc.)
Thank you.
To Apply:
At GlaxoSmithKline we provide a supportive working environment, and a
range of development challenges and opportunities. We also offer
competitive benefits and compensation packages designed to attract and to
retain the very best. For confidential consideration and efficient
processing, please apply online via our career pages at www.gsk.com.
Enter requisition number 30625 to be taken directly to this vacancy.
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