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DMC Biostatistician (EU Remote)

Employer
Cytel - EMEA
Location
Remote (Remote)
Salary
Competitive
Start date
22 Sep 2020
Closing date
22 Oct 2020

Job Details

Cytel provides unrivaled biostatistics and operations research knowledge to our customers in the life sciences industries in the form of both software and services. At Cytel, we work hard to create successful careers with significant professional growth for our employees, as a result of which they work hard to make Cytel successful. Cytel is a place where talent, experience and integrity come together to advance the state of clinical development.

 

We are experiencing exponential growth on a global scale in our Project-Based Services (PBS) team. You will support Phase I –IV clinical studies across a variety of therapeutic areas.  If you thrive working in a challenging, multi-tasking, deadline-driven environment, you will fit in well with our team of High Achievers!

 

This position can be for Senior/Principal/Associate Director levels, and provides statistical support for data collection design and analysis of clinical trial data, as specified by client contract in coordination with fellow team members.

 

Responsibilities:

  • Provides statistical support for data collection design and analysis of clinical trial data, as specified by the client contract, in coordination with the Project Director, Project Manager, Statistical Scientist Director and/or Statistical Scientist.
  • Provides guidance and oversight in producing statistical analysis and reports, including statistical sections of regulatory submissions, Data Monitoring Committee reports, and analyses for publication.
  • May serve as the primary statistician on projects, as needed.
  • Plans, develops and conducts project work as specified in the project contract in coordination with the Project Director, Project Manager, Statistical Scientist Director and/or Statistical Scientist.
  • Attends and may facilitate project team meetings on a regular basis.
  • Ensures blinding and security of data is maintained, as required by contract, charter, or protocol and in compliance with related SOPs.
  • Adheres to SOPs and applicable regulatory requirements, and ensures compliance among the project team.
  • Coordinates with the data management department for projects involving both clinical data management and statistical services.
  • Develops and facilitates internal and external presentations, as appropriate.

 

Qualifications:

  • Master’s degree in Biostatistics or Statistics
  • 8-10 years experience with design and analysis of experimental or clinical trial data
  • Expert level knowledge of statistical concepts with working knowledge of medical/scientific terminology
  • Strong organizational and multi-tasking skills are required, as are excellent verbal and written communication skills.
  • Must read, write and speak English. 

 

Physical, Mental & Sensory Requirements:

 

Ability to use computer keyboard/mouse; sit for long periods; see computer monitor and read; speak and listen.  Occasional long hours, and/or weekend/holiday hours.  75% of time spent at computer. Long and short term travel may be required, sometimes on short notice.

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