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ALLSTAT  2003

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Subject:

Job Vacancies at Novartis Pharma ag. Basel

From:

Natalie Fforde <[log in to unmask]>

Reply-To:

Natalie Fforde <[log in to unmask]>

Date:

Tue, 22 Jul 2003 17:36:36 +0100

Content-Type:

text/plain

Parts/Attachments:

Parts/Attachments

text/plain (84 lines)

Are you looking to work in a global growth company where you can make a
real difference? With about 77,200 associates around the globe in our
affiliates in over 140 countries, we share a vision of a better today and
tomorrow for patients - a vision that drives our growth and success. Our
greatest job satisfaction is knowing that we improve lives, we extend
lives, and we save lives - and we do it with increasing precision and
efficiency through breakthrough science and innovation.

Senior Statisticians for International Clinical Development
Pharma
Basel, Switzerland HQ
You will provide input to international clinical development plans, in co-
operation with the International Clinical Team. As a member of the
International Clinical Team, bring statistical expertise to the design,
analysis and reporting of clinical trials phases II to IV. The ideal
candidate will continuously strive for innovative solutions for our
studies. For this you will have access to a large international team of
statisticians in our Global Biostatistics group, and world-class internal
as well as external Methodology Consultants. As a senior Statistician, you
will ensure high scientific standards for studies, explore data for product
profiling, hypothesis generation, new research topics and publications, co-
ordinate project or study tasks with other statisticians and statistical
programmers.
Your qualifications:
l University degree in Statistics or Mathematics (Ph.D. or MSc. level)
l At least 5 years of relevant experience in the field of clinical trials
for the senior level, or at least two years for more junior levels are a
must
l Good knowledge of clinical trials methodology
l Knowledge of SAS and ideally some other alternative statistical software
l Flexible, positive, creative thinker, good communicator and negotiator,
team player.

Senior Statistician for Clinical Pharmacology
Pharma
Basel, Switzerland HQ
You will act as a member of International Clinical Pharmacology teams
bringing statistical expertise to the generation of pharmacological
concepts of early clinical development projects. Participate in the
planning and initiation of clinical studies by proposing design and
analyses in co-operation with other team members. The ideal candidate will
prepare analysis plans, implement exploratory and confirmatory analyses in
support of trial objectives and prepare statistical sections for clinical
trial reports, support the preparation of NDA integrated summaries of
effectiveness and safety, develop and implement novel statistical
procedures in design or analysis.

Your qualifications:
l MSc in Statistics
l At least 5 years’ experience in the field of Pharmaceutical Research and
Development
l Broad experience in experimental design, exploratory and confirmatory
data analysis
l Basic knowledge of pharmacological/physiological sciences and PK/PD
l Creativity, analytical thinking, good interpersonal skills and ability to
work in interdisciplinary teams
l Good knowledge of scientific computation and SAS, (S-Plus an advantage).

Senior Scientific SAS Statistical Programmers
Pharma
Basel, Switzerland HQ
You will assume responsibility for the production of statistical summaries
for clinical trials. Provide input to the specifications for analysis
datasets, pooled datasets, patient data listings, summary tables, and
figures using SAS tools. Furthermore, you will provide input into clinical
project documents (e.g. protocol, CRFs, and validation plans). Ensuring
quality of patient data listings, statistical summary tables and graphs by
implementing validation procedures and participating in multidisciplinary
and international clinical trial teams will also be part of your
responsibilities.
Your qualifications:
l Degree in a Life or Computer Science, Statistics or Mathematics
l Good knowledge of SAS and experience in using SAS in a scientific
environment
l At least 4 years of relevant experience in clinical trials are a must
l You need to be a team player with a continuous improvement mentality and
attention to detail.

For further information, contact Natalie Fforde, retained consultant,
Managing Director, Fforde-Management Ltd Curtis House, 34 Third Ave, Hove
BN3 2PD, Tel: 01273 722366, Fax: 01273 746954, Mobile: 07769 700 222.
Email: [log in to unmask]
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