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Senior Statistical Programmer/Analyst within the Clinical Pharmacology 
Statistics & Programming (CPSP) Department based in Harlow, Essex. An 
exciting opportunity exists for a Senior Statistical Programmer/Analyst 
within the Clinical Pharmacology Statistics & Programming (CPSP) 
Department based in Harlow, Essex.

As a key member of this international and dynamic team, you'll be working 
alongside medical statisticians and data scientists, performing and co-
ordinating analysis and reporting of clinical pharmacology trials data, 
together with associated regulatory submission work. Your main area of 
therapeutic focus will be Neurology and Psychiatry but there will be 
opportunities to work on studies in a variety of areas. 

You will be a graduate with a honours degree or MSc in statistics, 
computer science, or a related scientific or numerate subject, ideally 
with a minimum of 3 years experience within the pharmaceutical industry. 
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. Experience of SAS® is 
essential, however advanced SAS® training, if required, will be provided 
as well as specific clinical pharmacology area awareness. In this role you 
will be expected to : 

Work within clinical project teams in the planning and reporting of 
statistical summaries and analyses. This may include creation of analysis- 
ready datasets, including population PK datasets (these may be required 
for studies across all phases). 
Act as a department point of contact for customers in Clinical 
Pharmacology, clinical study teams, and across other departments in 
Biomedical Data Sciences (BDS) and attend meetings with senior staff 
within these groups as appropriate. 
Also act as study point of contact for study work contracted to CROs Have 
a clear analytical mind and knowledge of the software development 
lifecycle to input into the design development and maintenance of a 
library of statistical and other SAS programs, ensuring that these are 
validated and meet regulatory requirements. 
Use problem solving skills and an ability to think creatively to lead 
local process improvement projects and input into larger systems 
development projects managed by BDS technical groups and IT by helping to 
define detailed requirements and work with the team to achieve the most 
efficient and usable implementation of new systems. 
Work with staff in the other department locations in the UK and US, plus 
the UK outsourced operations to help review and prioritise workload. 


The variety of work undertaken by the team means that the successful 
applicant will have excellent workload management skills and be adaptable 
to changing priorities. Be able to act as a mentor or supervisor for more 
junior and contract staff. 

Please note that shortlisting preference will be given to applications 
received before 10th March 2006. Please use the "cover letter" of your 
online application to describe how 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.) Meanwhile 
thank you for your interest in this opportu