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Senior / Principal Biostatistician - Neuroscience FSP

Employer
Cytel - EMEA
Location
UK, Germany, Netherlands, Belgium, Spain,
Salary
Base salary plus annual performance bonus
Start date
7 Jun 2021
Closing date
7 Jul 2021

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Job Details

Cytel is a 100% biometric CRO. Join like minded people and enjoy work and life balance!

As a Senior/Principal biostatistician you will be responsible for statistical support, with a focus on ad-hoc work for clinical studies, and some publications support, across a variety of therapeutic areas in neuroscience.

You will participate in the development of study protocols including participation in study design discussions and sample size calculations, and review CRFs and data review guidelines.

Additionally, you will:

  • Develop statistical analysis plans (SAPs) including analysis dataset and TLG specifications
  • Perform statistical analyses
  • Interpret statistical results
  • Help prepare clinical study reports including integrated summaries for submissions

Why work with us?

  • Roles are very independent
  • Work with the client with a minimum supervision.
  • Lots of learning of therapeutic areas and indications
  • You have access to people who really understand particular diseases
  • Job allows you to learn how decisions are made at pharma companies
  • You would be involved in many activities
  • There are lots of promising studies
  • Using #SAS and #R
  • Work with supportive people

What we need from you:

  • MS or PhD in a science or industry-related discipline with five or more (8+) years working on clinical trials.
  • Experience in sample size calculation, protocol concept development, protocol development, SAP and preparing clinical study reports including integrated summaries for submissions.
  • Good SAS programming skills for QCing critical outputs, Efficacy/Safety tables and working closely with Programmers. 
  • Knowledge of R programming a plus.
  • Adept in ADaM specifications, generation and QC of datasets.
  • Submissions experience strongly desired.
  • Experience working with cross-functional teams, a Study Management Team (SMT) or similar teams for different clients.
  • Effective communicator: able to explain methodology and consequences of decisions in lay terms.
  • Team player; willingness to go the extra distance to get results, meet deadlines, etc.
  • Ability to be flexible when priorities change and deal with ambiguity.
  • Simulation and protocol design experience strongly desired.


It is a full time, permanent job

Recruitment process:

1. Video conversation with a recruiter
2. Video conversation with Director of biostatistics at Cytel
3. Video conversation with our pharmaceutical client

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