CONTRACT: Senior Statistical SAS Programmer
Statistical Reporting within Health Outcomes
6 months rolling contract
Location: Europe (Benelux) OR Atlanta, US
Job Summary:
For this major pharmaceutical client you will work with Health Outcomes
specialists (Patient Reported Outcomes Specialist, Epidemiologist, Health
Economist) and programmers based also in other sites. Primarily providing
programming support to Healthcare Outcomes and the Pharmaco-Epidemiology
team.
Accountabilities/Responsibilities:
* Provide programming support and validation of analysis data sets,
pooled datasets, statistical summary tables, figures and patient data
listings for phase I - III clinical trials, ISS & ISE, primarily using SAS.
* Provide output for the Clinical Study Report, the Integrated Summary
of Safety (ISS), the Integrated Summary of Efficacy (ISE), electronic
submissions and Exploratory Health Outcomes Research Reports.
* This position will require a significant training investment for the
use of client technology in relation to SAS macros, creation of analysis
data sets and dataset structures. Need for ensuring standardization of
programs where applicable.
* Apply knowledge of clinical data, the design and phases of clinical
trials, statistics, relevant regulations and the pharmaceutical industry to
the implementation of tasks.
* Handle complex statistical programming issues independently and be
familiar with study programming issues. Bring ideas for new projects and
take the initiative to solve issues.
Essential Skills & Capabilities:
At least X years Statistical SAS programming experience with prior
experience in pharmaceutical related field is required (experience with
large databases is an asset).
Working knowledge of clinical legislation (FDA, EMEA, ...), Good Clinical
Practice (GCP) and Clinical Data Interchange Standards Consortium (CDISC) is
a plus.
* SAS expert
* Statistical knowledge including basic statistics (descriptive
statistics, inferential parametric and non parametric analyses) and advanced
statistical techniques (multivariate analysis, ...).
* Fluent in English
* Ability to understand business problems rapidly and to reformulate
them in terms of appropriate statistical analyses to be performed.
* Ability to evaluate processes and situations in an orderly and
rational manner asking questions and identifying missing information.
* Accurately and efficiently work towards quality results
An excellent opportunity awaits for this renewable contract. Interview times
booked and full job specification to review...
If you would to discuss this role in greater detail or your application /
suitability to this or further roles, please call me or email me in
confidence. If you are not available or suited to this position, please feel
free to pass my details on.
We also have a broad variety of other Biometric specific vacancies available
in the UK and throughout Europe. Inclusive of SAS programming, Statistical,
Clinical programming, Data Management functions, Regulatory Affairs,
Clinical Research, QA, Compliance & Validation.
For a confidential consultation call James Carrera on 0044 (0) 207 255 6665
or email your CV to [log in to unmask]
James Carrera
European Manager
Pharmaceutical, Healthcare & CRO division
1st Pharma People
"A Division of 1st IT People"
Tel: +44 (0) 207 255 6665
Fax: +44 (0) 207 255 6656
mailto:[log in to unmask]
<mailto:[log in to unmask]>
www.1st-pharmapeople.com <http://www.1st-pharmapeople.com/>
This email is confidential and intended solely for the use of the individual
to whom it is addressed. Any views or opinions presented are solely those of
the author and do not represent those of the company from which the email
was sent. If you are not the intended recipient, be advised that you have
received this e-mail in error and that any use, dissemination forwarding,
printing or copying of this e-mail is strictly prohibited. While every
effort has been made to scan this e-mail, we can not accept any
responsibility for the loss of business or damage caused arising from this
email.
This email is confidential and intended solely for the use of the
individual to whom it is addressed. Any views or opinions presented are
solely those of the author and do not represent those of the company from
which the email was sent. If you are not the intended recipient, be advised
that you have received this e-mail in error and that any use, dissemination
forwarding, printing or copying of this e-mail is strictly prohibited.
While every effort has been made to scan this e-mail, we can not accept any
responsibility for loss of business or damage caused arising from this
e-mail.
|