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Senior Biostatistician

Alira Health
£43,414 - £54,972 a year
City of London, England
Full time
1 day ago
Are you being referred to one of our roles by a connection in Alira Health? If so, please apply using the referral link emailed to you.
Join our global team dedicated to innovation and initiative, where physical walls and different time zones don’t limit, but encourage, collaboration. Where all contributions and new ideas are explored with an open mind and work is driven by our shared values: be courageous, be accountable, be honest, be inclusive and elevate others.
Job Description Summary
The Senior Biostatistician carries out tasks assigned within the timelines and the standards of quality, while providing supervision to biostatisticians, preparing Statistical Analysis Plans and writing the statistical methodology and results sections of reports.
The Senior Biostatistician provides statistical input to the design and review of Protocols and Case Report Forms and prepares and performs trainings of other staff and clients on statistical methodology and statistical principles.
Job Description
THE SENIOR BIOSTATISTICIAN ROLE
The Senior Biostatistician carries out tasks assigned within the timelines and the standards of quality, while providing supervision to biostatisticians, preparing Statistical Analysis Plans and writing the statistical methodology and results sections of reports.
The Senior Biostatistician provides statistical input to the design and review of Protocols and Case Report Forms and prepares and performs trainings of other staff and clients on statistical methodology and statistical principles.
ESSENTIAL JOB FUNCTIONS*
  • Writes and reviews the statistical methodology and results sections of reports
  • Review of Statistical analysis (tables, figures and listings) and specifications of clinical trials
  • Performs sample size calculation
  • Writes Blind Review plans and reports
  • Writes and review statistical parts of scientific articles
  • Prepares and reviews Statistical Analysis Plans
  • Advises other staff and clients on statistical methodology and statistical principles.
  • Participates and conducts Blind Review meeting.
  • Supports the presentations to clients and manages the technical communications with client when assigned as lead statistician to a study
  • Create SAS and/or R programs for Datasets and TLFs validation
  • Prepares and performs training to internal/external staff on statistical methodology and statistical principles
  • Provides statistical input to the design and review of Protocols and Case Report Forms
  • Participates to DMC/DSMB meetings
  • Provides support to DMC/DSMB charter preparation
  • Reviews the specifications for analysis datasets
  • Conducts other activities as required
PREPARATION, KNOWLEDGE, SKILLS & ABILITIES
  • Master’s degree in Statistics
  • At least 3 years of experience in Biostatistics
  • SAS Programming, Good
  • R Programming, Basic/Good
  • Broad Range of Statistical methodology skills, Very Good
  • ICH E9 Statistical Principles for Clinical Trials, Very Good
  • English, Good
  • MS Office Suite, Good
  • Professional
  • Trustworthy
  • Ability to effectively prioritize
  • Quality focused
  • Personable Attitude
  • Willingness to learn
  • Team Player
  • Effective Stress Management Techniques
  • Learning Agility
  • Ability to Manage Conflict
  • Problem Solving Skills
  • Effective Verbal Communication Skills
  • Commercial and Technical Writing Skills
  • Networking Skills
Languages
English
Education
Bachelor of Arts (BA): Statistics
Contract Type
Regular
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