Manager, Clinical Statistics – World leading Pharma – King of Prussia, Pennsylvania

Manager, Clinical Statistics – World leading Pharma – $140 - $170k + Benefits – King of Prussia, Pennsylvania

Suitable for: Principal Statistician, Biometrics Manager, Senior Principal Biostatistician, Senior Statistician, Principal Research Biostatistician

Company/Department Background:

One of the world's leading pharmaceutical companies, with statisticians and programmers working at sites around the world. In recognition of the developing sophistication and technical requirements of the role of statisticians, the Clinical Statistics department was formed as a standalone department within the broader group, covering all phases of clinical drug development and commercialization in a wide range of therapeutic areas.

Please Contact Emily O’Brien on 646-569-9081 or email Emily.obrien@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

Position Summary:

Clinical Statistics is part of Quantitative Sciences, a group which includes clinical pharmacology modeling and simulation, epidemiology, non-clinical statistics, health economics modeling and statistical innovation.
This organization give their statisticians the opportunity to take part in world-class methodological research, as well as to fulfill a vital role on a multidisciplinary medicines development teams.
 

Manager, Clinical Statistics – World leading Pharma – $140 - $170k + Benefits – King of Prussia, Pennsylvania


Responsibilities of this Manager, Clinical Statistics includes:

  • Providing statistical input to the design, analysis, reporting and interpretation of clinical studies.
  • Influencing clinical development plans, regulatory and commercial strategies.
  • Building and maintaining effective strategic working relationships with internal and external partners to meet business needs.
  • Identifying, developing and implementing novel statistical methodologies in support of medicines development and product life-cycle management.
  • Study responsibility for a Large CV Outcomes Study


Requirements:

  • PhD or MSc(or equivalent) in a statistical discipline.
  • Experience in the design, execution, analysis and interpretation of clinical trials.
  • Expertise in a broad range of statistical methodologies.
  • Prior experience with pharmacokinetic and pharmacodynamic endpoints; and linear as well as nonlinear dose response modelling with application to real problems is a plus.
  • Demonstrated leadership and capabilities to reach across functional lines to support and manage a wide variety of tasks across different projects.

Please Contact Emily O’Brien on 646-569-9081 or email Emily.obrien@peoplewithchemistry.com if you would like to know more about this opportunity. This will be 100% confidential.

Keywords: Statistical, Statistician, Biostats, Biostatistics, Biostatistician, Statistics, SAS, Clinical, Drug, Development, Trial, Studies, Design, Analysis, Reporting, Data, Manager, Senior, Principal, Statistician, Biostatistician, Pharmaceutical, CRO, Pennsylvania, Philadelphia, King of Prussia, CDISC, SDTM, ADAM

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