An international pharmaceutical services company is currently seeking an experienced Biostatistician to be based in the Netherlands. This role will suit an individual who wants to take their career to the next level and join a rapidly growing team. The successful candidate will have the opportunity to work on all phases of clinical trials and have an exposure on various therapeutic areas.
Your responsibilities will include:
*Lead role in study design, helping to agree statistical timelines within the company
*Training and mentoring junior members of the team and subsequently perform quality assurance checks on their work
*Provide statistical advice for the study protocol and CRF design.
*Work closely with and project manage collaboration with statistical programmers and data managers
*Perform final quality checks on results submission before datalock
*Take responsibility for statistical documentation and use these to take a lead role in submissions
*Attending regular training and conferences, keeping up to date with the latest industry techniques
Experience and qualifications:
*Msc or PhD level in statistics, biostatistics, mathematics or equivalent
*Strong experience as a Statistician/Biostatistician within a pharmaceutical company, a biotech/biopharma or CRO
*Fluent in English (spoken and written)
*Sound SAS programming skills
*Excellent knowledge of clinical quality standards and protocols
*Experience of managing the statistical aspects of projects
*Excellent communication skills
To be considered for this role, please send your CV with a cover note to louise.beka@secpharma.com or for more detail on the role, please call Louise Beka on 0044 207 255 66 65