Biostatistician, Clinical Trials Design - Cape Town

Placements24

Cape Town

Sur place

ZAR 900 000 - 1 200 000

Plein temps

Il y a 11 jours

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Avantages offerts par ce poste

Competitive salary
Medical/dental/vision insurance
Retirement savings plan
Paid time off
Relocation assistance

Résumé du poste

Placements24 seeks a Biostatistician to join a pioneering pharmaceutical R&D team in Cape Town. You will design endpoints, sample sizes, and randomization schemes for clinical trials and provide SAPs and robust analyses using SAS, R, and SPSS.

You will mentor junior staff, ensure GCP compliance, and contribute to regulatory submissions and publications, supporting life-saving medical research from Cape Town.

Qualifications

  • Master's or Ph.D. in Biostatistics, Statistics, or a related quantitative field.

Responsabilités

  • Design statistically sound clinical trial protocols with endpoints, sample sizes, and randomization schemes.
  • Develop SAPs detailing methods for trial data analysis.
  • Perform complex statistical analyses on clinical trial data using SAS, R, or SPSS.
  • Interpret results and prepare regulatory submission reports and publications.
  • Provide statistical expertise to investigators and study teams.
  • Ensure compliance with GCP, FDA/EMA guidelines and internal SOPs.
  • Critically review literature and proposals for statistical validity.
  • Contribute to development and validation of statistical methods.
  • Assist in manuscript preparation for journals and conferences.
  • Mentor junior biostatisticians and programmers.

Connaissances

Biostatistics
Clinical trial design
Survival analysis
Longitudinal analysis
SAS
R
CDISC SDTM/ADaM
Regulatory knowledge
Statistical programming
Communication

Formation

Master's or PhD in Biostatistics or related

Outils

SAS
R
SPSS

Description du poste

Placements24 seeks a Biostatistician to join a pioneering pharmaceutical R&D team in Cape Town. You will design endpoints, sample sizes, and randomization schemes for clinical trials and provide SAPs and robust analyses using SAS, R, and SPSS.

You will mentor junior staff, ensure GCP compliance, and contribute to regulatory submissions and publications, supporting life-saving medical research from Cape Town.

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