Parexel Uxbridge, England, United Kingdom
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Parexel Uxbridge, England, United Kingdom
3 days ago Be among the first 25 applicants
Join to apply for the Senior Biostatistician role at Parexel
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
Seniority level
* Seniority level
Mid-Senior level
Employment type
* Employment type
Full-time
Job function
* Job function
Research, Science, and Analyst
* Industries
Pharmaceutical Manufacturing, Biotechnology Research, and Hospitals and Health Care
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