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Senior Principal Biostatistician

Employer
Parexel
Location
Sheffield, United Kingdom
Salary
Competitive
Start date
17 Oct 2019
Closing date
16 Nov 2019

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Job Details


As a Senior Principal Biostatistician, you will lead research design and analytical strategies, input into protocols, develop and review statistical analysis plans and author/co-author reports, abstracts and manuscripts and provide statistical advice. You will input into the quality control of statistical deliverables. As the Functional Lead within a study team, you will lead the biostatistical and statistical programming activities on a study and be accountable for the deliverables from these functions. Key responsibilities also include; project management of deliverables, resource and function specific budget. You will have the opportunity to become a subject matter expert for specific tasks within a key client partnership and to become involved in business development activities.

In this role you may;
  • Perform or supervise complex statistical analyses and create or provide input to statistical reports.
  • Cooperate with other biostatistical and company departments to optimize global efficiency.
  • Act as a pro-active advisor for all types of analysis during the proposal process as well as during the project life cycle; define strategies and evaluate the statistical resources needed to meet the defined goals.
  • Coordinate Biostatistics related project activities for successful completion within given timelines and budget.
  • Interact with clients with regard to data analysis, scope of work, and budget.
  • Review derived datasets and all types of statistical analysis deliverables.
  • Develop complex analysis strategies and execute them using efficient programming techniques (software: SAS, R).
  • Produce and provide expert input to analysis plans, statistical reports, statistical sections of integrated clinical reports and other process supporting documents.
  • Quality control of all kinds of statistical deliverables.
  • Train/mentor junior members of the department.
  • Represent Parexel at client meetings.


Qualifications

  • Masters or PhD in a statistical discipline.
  • A thorough understanding of the statistical aspects of both clinical trials and observational studies.
  • Experience in statistical analysis in a clinically related subject, either within clinical trials or in Epidemiology. This can be either within academia or professionally - and/or in Outcomes Research.
  • Confidence, be self-reliant and a quick learner who enjoys working in a matrix team.
  • You ideally have advanced SAS programming skills, but this is not necessarily essential.
  • Strong oral and written English communication skills.
  • Ability to travel as required, although this is not frequent.

Company

Trialing new treatments. Advancing healthcare. Reinventing medicine as we know it. When you join us, you’re joining a team that sees everything they do as an opportunity to transform the world for patients everywhere. When our employees bring their many perspectives together to tackle a new challenge, there’s no limit to what they can accomplish. Through it all, at the center of all we do, is a patient whose life could change – forever. And together, we’ll do it With Heart™.

Parexel is among the world’s largest clinical research organizations (CROs), providing the full range of Phase I to IV clinical development services to help lifesaving treatments reach patients faster. Leveraging the breadth of our clinical, regulatory, and therapeutic expertise, our team of more than 21,000 global professionals works in partnership with biopharmaceutical leaders, emerging innovators, and sites to design and deliver clinical trials with patients in mind, increasing access and participation to make clinical research a care option for anyone, anywhere. 

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Company info
Website
Telephone
+44 1895 238000
Location
The Quays
101-105 Oxford Road
Uxbridge
Middx
UB8 1LZ
United Kingdom

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