Hybrid Principal Biostatistician Consultant

Posted 17 hours ago

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About the role

  • Principal Biostatistician Consultant at ClinChoice overseeing drug development statistical methodologies. Lead statistician for clinical studies in a hybrid work environment.

Responsibilities

  • Work with Biometrics director to manage one or more compounds/Indications in R&D for the entire life cycle.
  • Responsible for all statistical aspects of the drug development and/or post-approval programs.
  • Coordinate statistical and programming support and manage contractors/CROs when necessary.
  • Serve as lead statistician for clinical studies and collaborate effectively with the study team members.

Requirements

  • M.S. or Ph.D. (or equivalent) in Statistics or Biostatistics is required.
  • Minimum 4 years (Ph.D.) or 8 years (M.S.) pharmaceutical industry experience
  • Should possess experience interacting with regulatory agencies (e.g. FDA, MHRA or EMEA).
  • Experience managing multiple projects/therapeutic areas.
  • Experience in managing external vendors (e.g. contractors, CROs).
  • Capability in working independently and lead one or multiple clinical studies.

Benefits

  • Competitive salary
  • Hybrid work arrangement
  • Opportunities for professional development
  • Access to a supportive culture

Job title

Principal Biostatistician Consultant

Job type

Experience level

Lead

Salary

Not specified

Degree requirement

Postgraduate Degree

Location requirements

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