Senior Biostatistician — Remote, Impactful Trials Leader

Warman O'Brien

Poland

On-site

PLN 200,000 - 320,000

Full time

8 days ago
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Benefits offered by this job

Fully remote
Flexible schedule

Job summary

Warman O'Brien is seeking a Senior Biostatistician to lead biostatistical and programming activities for studies of moderate complexity in a fully remote setting across UK/Europe. The role emphasizes delivering high-quality analyses, collaboration with cross-functional teams, and the ability to translate complex statistics for stakeholders.

The ideal candidate will hold an M.S./Ph.D. in Statistics or Biostatistics with 5+ years in a CRO/pharma environment, strong SAS skills, and excellent

Qualifications

  • Requires an M.S. or Ph.D. in Statistics/Biostatistics or related field.
  • 5+ years’ experience in biostatistics within a CRO/pharma setting.
  • Strong applied parametric/nonparametric stats and SAS programming.
  • Deep knowledge of study designs and clinical trial methodology.
  • Excellent written and verbal communication.
  • Ability to translate complex stats for non-technical stakeholders.

Responsibilities

  • Lead statistical tasks for studies of moderate complexity.
  • Contribute to protocol development and sample size calculations.
  • Design CRFs with statistical input.
  • Create SAPs and derived data definitions.
  • Prepare tables, listings, and figures for CSRs.
  • Ensure consistency across a program of studies.
  • Write the statistical methods sections of reports.

Skills

M.S./PhD in Statistics
CRO experience
SAS programming
Study design knowledge
Communication skills
Clinical trial methodology

Education

M.S./Ph.D. in Statistics or Biostatistics

Tools

SAS

Job description

Warman O'Brien is seeking a Senior Biostatistician to lead biostatistical and programming activities for studies of moderate complexity in a fully remote setting across UK/Europe. The role emphasizes delivering high-quality analyses, collaboration with cross-functional teams, and the ability to translate complex statistics for stakeholders.

The ideal candidate will hold an M.S./Ph.D. in Statistics or Biostatistics with 5+ years in a CRO/pharma environment, strong SAS skills, and excellent

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