Senior Statistical Analyst in Cambridge

Senior Statistical Analyst in Cambridge

Cambridge Full-Time 63000 - 77000 £ / year (est.) No working from home possible
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At a Glance

  • Tasks: Lead statistical analysis on real-world evidence trials and develop impactful reports.
  • Company: Join a leading global CRO with a dynamic and collaborative culture.
  • Benefits: Enjoy flexible working, competitive salary, and a comprehensive benefits package.
  • Other info: Experience excellent career growth and a supportive work-life balance.
  • Why this job: Make a difference in healthcare through innovative statistical analysis and real-world evidence.
  • Qualifications: Master's or PhD with 5+ years in statistics or SAS programming, preferably in pharma.

The predicted salary is between 63000 - 77000 £ per year.

  • Senior Statistical Analyst (RWE) – Global CRO – Remote or Office Based – UK/Europe
  • APPLICANTS WITH PHARMA BACKGROUND NEED ONLY APPLY

We have partnered with this leading, global CRO, who are looking for a Senior Statistical Analyst within their Real World Evidence strategy & analytics team - (office or Home based) to join their dynamic and exciting team, where you will be dedicated to working on observational and real world evidence based trials for a number of indications.

As the Senior Statistical Analyst, you will develop statistical analysis plans and perform statistical analysis on assigned projects in accordance with study specifications, applicable guidelines, regulatory requirements and SOPs.

In addition, you will be responsible for producing the tables, listings and figures for studies, manuscripts and abstracts, as well as operating in a client facing role and act as a project lead across the team.

You will be expected to recognize the importance of and build a culture of process improvement with a focus on streamlining our processes adding value to the business and meeting clients' needs.

Location

Office based, or home based across the UK or Europe

Role Responsibilities

  • Supports study start-up activities (e. g. reviews, comments on and contributes to study design, protocols, case report forms).
  • Writes statistical methods sections of study protocols including sample size and power calculations with oversight.
  • Supports development of statistical analysis plans and develops table shells.
  • Reviews database specifications and leads initial review of raw variables and develops written specifications for derived variables from oral descriptions.
  • Programs basic statistical procedures and specialized statistical procedures (e. g., repeated measures, survival analysis, etc.) and/or SAS/Graph.
  • Develops complex macros for use by the group.
  • Develops deliverables, such as project reports and outputs, graphs, and tables with oversight.
  • Writes methods and results sections of final reports and publications such as abstracts, presentations, and manuscripts, with oversight.
  • Communicates with the client or investigator as needed.
  • May participate in professional activities including presentations at technical conferences (e. g. SAS meetings, ISPOR) with oversight.

Person Specification

  • Master's or Ph D
  • 5+ years of experience as a Statistician or SAS Programmer
  • Prior clinical industry experience in either CRO, pharmaceutical, or academic/site setting
  • Proficient in SAS Data step with simple and complex conditional statements and variable creation, merges and concatenation
  • Experience using macros and arrays for repetitive tasks.
  • Experience using descriptive statistics procedures for summarizing, restructuring, and outputting data.
  • Experience using SAS Output Delivery System to control output from statistical procedures.
  • Proficient in performing analyses using basic through advanced statistical procedures.
  • Prior real world study experience is preferred, but not required.

They offer

  • Competitive salary
  • Flexible working options
  • Very competitive benefits package
  • Excellent career development opportunities
  • Supportive policies and wellbeing initiatives for you and your family

What is in it for you?

  • Interesting and innovative projects
  • Collaborative and inspirational working environment / atmosphere
  • Excellent career development and progression opportunities
  • Be challenged in a fast-paced team environment that is collaborative in performing biostatistical analyses and statistical programming.
  • Development opportunities and mentoring at all levels enable you to progress your long-term career in the direction you choose.
  • Work – life balance
  • WFH or office based.

What to do next: If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome the new Statistical Analyst onboard as soon as possible.

Senior Statistical Analyst in Cambridge employer: Warman O'Brien

Join a leading global biotech organisation that is at the forefront of Oncology innovation, where your expertise as a Senior Medical Science Liaison will be valued and impactful. With a hybrid work model, you will enjoy a flexible work-life balance while being part of a collaborative culture that prioritises employee growth and development through continuous learning opportunities. This role not only offers competitive benefits but also the chance to contribute to groundbreaking advancements in healthcare, making it a truly rewarding career choice.

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Contact Details:

Warman O'Brien Recruitment Team

StudySmarter Expert Advice🤫

We think this is how you could land Senior Statistical Analyst in Cambridge

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We think you need these skills to ace Senior Statistical Analyst in Cambridge

Statistical Analysis
SAS Programming
Statistical Analysis Plans
Sample Size Calculations
Power Calculations
Database Specifications Review
Statistical Procedures (Basic to Advanced)

Some tips for your application 🫡

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How to prepare for a job interview at Warman O'Brien

✨Brush Up on Lab Techniques

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