Project Statistician - Germany
My Client is a Global Pharmaceutical company with headquarters in Germany and are currently looking for a Project Statistician to join their Biometrics team.
Job Description:
Providing statistical input at the clinical project and trial level in alignment with the overall clinical
strategy
Applying statistical modeling, simulation, predictions and analysis methods for
optimizing trial designs and clinical development programs
Writing statistical analysis plan, conducting data analyses, interpreting, presenting and reporting
statistical results
Providing input to the clinical part of regulatory documents and representing statistics at
regulatory authorities and in the scientific community
Cooperating with Clinical Research Organizations
Working according to ICH-GCP and ICH-biostatistics guidelines
Instructing and supervising Trial Biostatisticians and Biostatistical Programmers
Requirements:
A minimum 5 years experience in biostatistics in the pharmaceutical industry
BSc in mathematics/statistics, biometry or equivalent degree
You have experience at interacting with very senior levels and effective at interacting with all
levels of employees across highly matrixes organization
Proficient verbal and written skills in English are required.
If you are interested in this opportunity please send a copy of your CV to [log in to unmask] or call 0044 (0) 207 822 1710
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Senior Statistician - Germany
My Client is one of the most predominant names within the Pharmaceutical development sector with a global reach and outstanding reputation for delivering the highest quality clinical research work. As the company are expanding globally they are looking for a Biostatistician to join their established Statistics Team to ensure that their reputation for delivering high quality results are upheld.
Job Description:
• Handling of all statistical methodological issues for newly registered drug projects
• Providing expert statistical advice to clinical project physicians from our
Corporate Medical Affairs and Drug Safety departments
• Working in international drug development teams and collaborating with
external opinion leaders
• Statistical planning and review of drug development programmes for launch and
drug profiling activities including protocol development for major phase IIIb/IV
studies
• Statistical planning and review of drug product publication plans, health
technology assessments, risk management plans and pharmacovigilance reports
• Planning and performing exploratory analyses of existing study data for publications,
reimbursement negotiations, drug defense strategies and further
development planning
Requirements:
MSc or PhD in statistics or mathematics
Comprehensive working knowledge of biostatistical methodology
based on a successful career as a statistician in international clinical drug
development for several years.
If you are interested in this opportunity please send a CV to [log in to unmask] or call +44 (0) 207 822 1710
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