Job Description

When our values align, there’s no limit to what we can achieve.
At Parexel, we all share the same goal – to improve the world’s health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special – a deep conviction in what we do.

Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we’re committed to making a difference.

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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