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Senior Biostatistician

United Kingdom, Remote 职位编号 R0000035010 类别 Biostatistics Jobs
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关于这个职位

We are currently hiring a Biostatistician to join our FSP Team! This individual will provide statistical support for projects in the Vaccines Therapeutic Area. The successful candidate will collaborate and work closely with project / study teams and provide statistical expertise in designing research concepts, developing protocols, writing statistical analysis plans, performing statistical analyses, interpreting and presenting results, writing/reviewing reports, and publishing manuscripts through co-authorship.  The candidate may also provide support in regulatory submissions including responses to regulatory queries. 

In this role you will;

  • Provide scientifically rigorous statistical input on post-hoc / ad-hoc analysis requests in supporting publication projects and regulatory query responses.

  • Develop statistical analysis plans, mock-up tables, quality check plans.

  • Oversee programming support activities for assigned projects.  Validate the accuracy, consistency and integrity of the statistical output displays generated by programmers.

  • Lead multiple project teams by applying project management skills, statistical and programming techniques to prepare, execute, report, and document of high-quality statistical analysis per statistical analysis plans.

  • Conduct peer review of project related work performed by other statisticians, maintain compliance with the latest regulatory requirements, maintain project documentation and files according to departmental policy.

  • Communicate competently and independently with client to coordinate the statistical and programming considerations of the project.

  • Demonstrate strong understanding of ICH guidelines and clinical trial design, as applicable to statistics.

You will have;

  • Masters in Statistics/Biostatistics (or related field) with 8+ years’ experience in clinical trials, or PhD in Statistics/Biostatistics (or related field) with 4+ years’ experience in clinical trials.

  • Effective verbal and written communication skills

  • Understanding of broad statistical theory and its application

  • Able to fully understand clinical questions and concepts and to translate and simplify them into SAP development followed by data generation all the way through publication. 

  • Effective at clearly explaining statistical concepts to colleagues without statistical training

  • Experience with statistical modelling of clinical data and statistical inference

  • Experience in R or SAS programming languages

  • Experience with different study designs, protocol development, and statistical analysis plan writing

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