Are you looking to work in a global growth company where you can make a
real difference? With more than74,000 associates around the globe in our
affiliates in more than 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.
The Biostatistics Section in Clinical Research and Development of Novartis
Pharma AG, Basel (Switzerland) is looking for:
Senior Statisticians for International Clinical Development
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
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
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:
University degree in Statistics or Mathematics (Ph.D. or MSc. level)
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
Good knowledge of clinical trials methodology
Knowledge of SAS and ideally some other alternative statistical software
Flexible, positive, creative thinker, good communicator and negotiator,
team player.
Senior Statistician for Clinical Pharmacology
You will:
Act as a member of International Clinical Pharmacology teams
Bring 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
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:
MSc in Statistics
At least 5 years experience in the field of Pharmaceutical Research
and Development
Broad experience in experimental design, exploratory and confirmatory
data analysis
Basic knowledge of pharmacological/physiological sciences and PK/PD
Creativity, analytical thinking, good interpersonal skills and ability
to work in interdisciplinary teams
Good knowledge of scientific computation and SAS
S-Plus of advantage.
WE WILL CONSIDER APPLICATIONS FROM ANYWHERE IN THE WORLD, WORK PERMITS AND
RE-LOCATION IN AVAILABLE, PLEASE CONTACT NATALIE FFORDE FOR FURTHER
INFORMATION
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
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