PHASTAR are a team of expert statisticians and programmers, working in the
medical field. There are a number of reasons you may wish to join the
PHASTAR team:

1. Learn from PHASTAR's internal experts. We have a number of personnel with
more than 20 years experience, and a number of staff with PhDs in specialist
areas.
2. A better way to work: PHASTAR have a unique approach to statistical
consulting and data analysis that you will be taught. Our approach ensures
high quality consulting and data analysis.
3. A relaxed place to work. PHASTAR encourages a hard working but friendly
and sociable office environment.

We are looking to employ statisticians and SAS programmers with at least 3
years experience to get involved in the design, analysis and reporting of
clinical trials.
We can offer:

. Advancement of your career in an intellectually-stimulating, dynamic,
supportive environment . Variety of projects in statistical consultancy and
clinical trial reporting (range of therapeutic areas and phases) . Excellent
remuneration (competitive salary, pension, healthcare, conferences and
courses etc)

PHASTAR will consider sponsoring visas for candidates with the right
experience.

SAS Programmers
We are looking for SAS programmers with at least three years experience,
ideally in a clinical trials environment. You would have experience in
manipulating data using Base SAS programming as well as producing reports
(tables and graphics) using a variety of procedures. You should be
comfortable using macros, and experience in the process of production and
quality control of clinical trial outputs. The ideal candidate would also
have knowledge of CDISC, in particular SDTM and AdAM standards.

Senior Statisticians
If you would like to work with a team of expert statisticians, in a company
run and managed by statisticians, where your skills will bevalued and
nurtured, then our roles may be right for you. We are seeking medical
statisticians, with at least three years experience, ideally in a clinical
trials environment. You would have experience manipulating, summarising and
analysing clinical trials data using a variety of statistical methods. The
ideal candidate would also have experience in setting up clinical trials and
have a masters degree or doctorate in a statistics related discipline.

PHASTAR provides statistical consulting and clinical trial reporting
services to small biotech and corporate pharmaceutical companies.

PHASTAR
Our number one priority is to ensure that the work we produce is of the
highest quality: every project PHASTAR undertakes is supervised on
methodology and utilises internal processes designed to ensure optimal
quality. Additionally, we have operational measures to ensure that the vast
experience of our team is leveraged into every single report that we
produce.

Services include production of TFLs, study design, modeling and simulation,
analysis planning, CDISC services, meta-analysis, advice on handling missing
data across phase I to IV trials. We are based in West London, UK and work
with companies across Europe and the US.

We can work with our own internal systems and processes or seamlessly
incorporate with your teams. We can manage and deliver whole clinical trial
programs, or provide statistical advice on a trial that you are planning.
Our vision is to become the supplier of choice for specialist statistics
services to the pharma and biotech sector, by delivering quality advice and
results, on time and on budget.

To apply or arrange a confidential chat, please contact PHASTAR HR manager
[log in to unmask] or call 0207 183 7062

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