
Proven experience within an HEOR /Regulatory Biostatistics position and training (to PhD or Masters level) within Biostatistics or a similar quantitative analysis subject are essential pre-requisites. Applicants may have previously worked for either a pharmaceutical / biotechnology manufacturer or a life sciences consulting organisation but a detailed understanding of regulatory submission requirements in the USA and proven project management skills are vital.
Applicants must be able to demonstrate a blend of scientific, technical (statistical analysis), leadership and communication skills and be comfortable working in a client-facing role. If you have substantial experience within biostatistics for clinical trial design and regulatory evidence generation as well as proven strategic leadership skills, this is an excellent opportunity for you.
Apply today to arrange a confidential discussion about this opportunity.(Applicants must be legally authorized to work in the USA. Applicants requiring visa sponsorship may be considered)
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