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Senior Statistical Programmer FSP

Cytel

Role overview

Qualifications

  • Advanced SAS programming skills
  • Proficiency in CDISC standards (SDTM, ADaM)
  • Experience in Phase I-IV clinical trials

Responsibilities

  • Support or lead one or more Phase I-IV clinical trials
  • Work fully embedded within a pharmaceutical client
  • Collaborate with diverse perspectives in a team environment
  • Leverage advanced programming skills to innovate solutions

Key facts

Hard skills

Other skills

  • Collaboration
  • Problem Solving
  • Intellectual Curiosity
  • Innovation

About the company

Cytel logo

Cytel

  • Clinical Research (CRO)
  • Large
  • 1,001–5,000
Cytel Inc., an advanced analytics leader with over thirty years of experience providing sophisticated quantitative insights to executive decision-makers in the lifesciences. Cytel employs a range of data science tools from biostatistics to machine learning to help executives in the life-sciences to make confident decisions powered by data. We are probably best known for being leaders in the field of adaptive clinical trial design, a subset of trial design that uses interim looks to enhance the patient safety and commercial value of pharmaceutical products. We also have specialists in Bayesian statistics, real world evidence, artificial intelligence, health economics, and a number of other research fields to ensure that academic and scientific findings can have impact on industry quickly and seamlessly. www.cytel.com
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Job description

Sponsor-dedicated: Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program.
 Position Overview: 
 As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote.
 Our values
  • We believe in applying scientific rigor to reveal the full promise inherent in data.
  • We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery.
  • We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities.
  • We prize innovation and seek intelligent solutions using leading-edge technology.

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