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Based in Berlin, Germany.

in Germany - home-based

Permanent

Start date: As soon as possible

Role and responsibilities

Ability to lead a team of statisticians and programmers to manipulate, summarise and analyse clinical trial data using a variety of statistical methods, ultimately delivering clinical trial results to an agreed timeline with optimal quality
Project management responsibilities, including allocating staff, predicting and planning resources
Preparation and review of study documentation e.g. protocols and statistical analysis plans
Ability to advise, mentor and teach both internal and external statisticians with regards to statistical and data analysis methods
Function as a study expert across a number of studies, helping to clarify details on analysis methods for the internal PHASTAR team
Responsible for ensuring the team meets the highest quality standards, and follows the principles detailed in PHASTAR's internal procedures
Maintaining a positive and engaging client relationship with regards to statistical issues

Experience

PhD or MSc in Biostatistics or related discipline
Experience working within a clinical trials environment (Pharma, CRO or academic)
Previous experience performing statistical analysis using SAS
Excellent written and verbal communication skills
Ability to communicate with a broad range of people across different functions

You must be eligible to work in Germany for this position.

To apply please fill out the form below, or alternatively phone +44 (0)20 7183 7061.

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