Hybrid Biostatistician: Clinical Trials Data Analysis (SAS)

Placements24

Stellenbosch

Hybrid

ZAR 900,000 - 1,300,000

Full time

8 days ago

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Benefits offered by this job

Competitive salary package
Medical aid
Retirement planning
Life insurance
Training and conference opportunities
Career advancement

Job summary

Placements24 is seeking a Biostatistician in Stellenbosch, Western Cape for a hybrid role. You will design trials, develop SAPs, and perform analyses using SAS and R, ensuring regulatory compliance and rigorous interpretation of results.

The role requires a Master’s or PhD in Statistics/Biostatistics with 4+ years in pharma/biotech clinical trials, plus CDISC familiarity. Collaboration with clinical, data management, and regulatory teams is essential.

Qualifications

  • Master's or Ph.D. in Statistics, Biostatistics, or a related quantitative field.
  • Excellent analytical, problem-solving and communication skills.
  • Strong understanding of clinical trial design, data analysis techniques, and regulatory requirements.

Responsibilities

  • Design clinical trial protocols with statistical input, including sample size and endpoints.
  • Develop Statistical Analysis Plans (SAPs) and analyses using SAS/R.
  • Prepare statistical reports for internal stakeholders and regulatory submissions.
  • Interpret analysis results and ensure data integrity across trials.
  • Mentor junior biostatisticians and collaborate with cross-functional teams.

Skills

Analytical thinking
Communication
Problem-solving

Education

Master's or PhD in Statistics/Biostatistics

Tools

SAS
R
CDISC

Job description

Placements24 is seeking a Biostatistician in Stellenbosch, Western Cape for a hybrid role. You will design trials, develop SAPs, and perform analyses using SAS and R, ensuring regulatory compliance and rigorous interpretation of results.

The role requires a Master’s or PhD in Statistics/Biostatistics with 4+ years in pharma/biotech clinical trials, plus CDISC familiarity. Collaboration with clinical, data management, and regulatory teams is essential.

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