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Senior Statistician

Description:
This is a part-time (3 days a week) position for a senior statistician with significant industry experience. As a clinical statistician, you’ll help prepare timely, reliable and appropriate processing of the statistical evaluation for clinical study projects. You’ll also be generating output of clinical data supplied electronically by Clients, according to ICH, GCP, Standard Operating Procedures (SOPs) and client instructions.

What You’ll Learn:
You’ll expand your statistical analysis skills and learn to think creatively to solve client issues and to uncover the best way to get to the data the client wants. You’ll have the opportunity to explore topics like adaptive clinical trials and to expand your analytical background.

All our employees also benefit from the unique team environment and a corporate culture that is specifically focused on your growth and development. You’ll learn what it means to be a productive member of a team, how to support international colleagues, and how to manage projects big and small through to completion. Most importantly, you’ll learn the true satisfaction of providing quality service and support to customers from an organization that strives to make every client interaction exceptional.

Responsibilities:

  • Responsible for all aspects of trial analysis from statistical analysis plans and randomisations through to analysis and direct input into clinical trial reports
  • Programming, in SAS®, of hypothesis tests and tables/figures/listings/analysis datasets as appropriate
  • Work with Electronic Data Capture systems and real time data
  • Assist in the development of Datatrial SOPs, maintain and improve systems as appropriate
  • Train DM staff in the use of SAS for data validation

Requirements:

  • Qualified to degree level, preferably MSc with a strong statistical background
  • 4-10 years in a CRO or Pharma environment
  • Experience of reporting in SAS essential
  • Phase I/II and multinational Phase III work experience preferable
  • Experience of working with CDISC datasets would be beneficial
  • Good organisational skills; good communication skills (oral and written); analytical skills; attention to detail
  • Ability to work towards tight deadlines
  • Able to work as part of a team or individually
  • SAS Skills: Base SAS, SAS Macro, SAS Stat
  • The candidate would work on all phases of clinical trials in many therapeutic areas and possess the flexibility and “hands-on” approach, as well as technical expertise, to suit the CRO environment 

If this sounds like you, drop us a note and let’s explore your future with Datatrial.

E-mail us your cover letter and resume to careers@datatrial.com.

*Direct applicants are welcomed and encouraged.