Overview

We currently have openings for Senior and Principal Statisticians based in Cyprus to join our Employee- Owned Biostatistics CRO, Plus-Project. All opportunities are under the FSP model; hence you must feel comfortable working in this environment & ideally have prior experience. 

Plus-Project are excited to announce that we currently have openings for experienced Senior and Principal Statisticians based in Cyprus. All opportunities are under the FSP model; hence you must feel comfortable working in this environment & ideally have prior experience. The ability to perform a lead study statistician role is essential; study design or Bayesian experience is desirable

Key Responsibilities

• Act as lead statistician for multiple projects with any level of complexity.
• Collaborate in the process of protocol development by choosing an appropriate study design, including statistical methodologies, calculating necessary sample size to achieve a pre-specified power, and writing the statistical section of the protocol.
• Collaborate cross-functionally with study teams members to effectively deliver high-quality results.
• Perform statistical review of relevant study documentation (i.e. case report form, randomisation specification, dataset specifications) and clinical study reports.
• Author and review Statistical Analysis Plans (SAPs) based on the protocol, including development of output shells for tables, figures and listings.
• Programming and QC of efficacy analysis datasets and associated tables, figures and listings.
• Participate in Data Safety Monitoring Board and/or Data Monitoring Committee activities, including charter development.
• Prepare key portions of the integrated clinical/statistical report, ISS and ISE, including sections related to data handling and statistical methodology, patient accountability, baseline compatibility, and efficacy results.
• Principal Statistician (in addition to above): provide expert leadership to internal and external study teams in the reporting of clinical trials data, regulatory submissions, safety updates and publications.

Skills & Experience

• Master's Degree or PhD in Statistics (or related discipline)
• Excellent oral and written communication skills
• Excellent analytical skills
• Proficiency in SAS / R programming languages
• Ability to apply knowledge of statistical design, analysis and programming techniques used in clinical trials
• Senior Statistician: At least 4 years of experience working as a Statistician in clinical drug development with project leadership experience
• Principal Statistician: At least 8 years of experience working as a Statistician in clinical drug development with strong demonstrable project leadership experience
  

How to Apply

Click here to apply!