Hybrid Pharmaceutical Biostatistician — Clinical Trials Expert

Placements24

Queenstown

Hybrid

NZD 110,000 - 160,000

Full time

4 days ago
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Benefits offered by this job

Competitive salary
Health and wellness benefits
Retirement savings plan
Professional development opportunities

Job summary

Placements24 in Queenstown is seeking a highly skilled Pharmaceutical Biostatistician to lead design, analyses, and regulatory support for clinical trials in a hybrid on-site/remote setting.

You will work with cross-functional teams, develop Statistical Analysis Plans (SAPs), perform analyses in SAS and R, and communicate results to statisticians and non-statisticians. A strong regulatory and trial-design foundation is required.

Qualifications

  • Master's degree or PhD in Statistics, Biostatistics, or a related quantitative field.
  • 4+ years of biostatistics experience in pharma/biotech environment.
  • Proficiency with SAS, R, or SPSS and strong regulatory knowledge.

Responsibilities

  • Design clinical trial protocols with robust statistical methods and sample sizes.
  • Develop SAPs outlining endpoints for studies.
  • Perform statistical analyses using SAS or R.
  • Interpret results and communicate insights to teams.
  • Prepare CSRs and regulatory submission documents.
  • Collaborate with data management to ensure data integrity.
  • Consult with investigators on statistical matters.
  • Stay current with regulatory guidelines and methods.
  • Present findings at meetings or conferences.
  • Contribute to research strategy and evaluation of new candidates.

Skills

Statistical analysis
Clinical trial design
Data interpretation
Analytical thinking
Communication skills

Education

Master's degree in Statistics or Biostatistics
PhD in Statistics/Biostatistics

Tools

SAS
R
SPSS

Job description

Placements24 in Queenstown is seeking a highly skilled Pharmaceutical Biostatistician to lead design, analyses, and regulatory support for clinical trials in a hybrid on-site/remote setting.

You will work with cross-functional teams, develop Statistical Analysis Plans (SAPs), perform analyses in SAS and R, and communicate results to statisticians and non-statisticians. A strong regulatory and trial-design foundation is required.

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