Remote Biostatistician – Clinical Trials Insights

Placements24

Gqeberha

Hybrid

ZAR 900,000 - 1,200,000

Full time

2 days ago
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Benefits offered by this job

Fully remote work
Health and wellness benefits
Online courses & conferences
Retirement savings plan
Flexible working hours

Job summary

Placements24 is seeking a Biostatistician to join a remote team in South Africa. The role focuses on designing, analyzing, and interpreting clinical trial data using SAS or R, contributing to regulatory submissions and publications.

The ideal candidate holds a MSc/PhD in Statistics or Biostatistics with at least 4 years in biostatistics within pharma/biotech, and a solid grasp of CDISC SDTM/ADaM. Remote work from anywhere in South Africa is offered.

Qualifications

  • Master's or Ph.D. in Statistics, Biostatistics, or a closely related quantitative field.
  • Minimum 4 years of biostatistics experience in pharma/biotech with clinical trials.
  • Proficiency in SAS or R for analysis and reporting.
  • Strong understanding of clinical trial design and regulatory requirements (ICH).
  • Experience with CDISC standards (SDTM/ADaM) is a plus.

Responsibilities

  • Design SAPs for clinical trials in collaboration with development teams.
  • Perform SAS or R analyses for efficacy and safety across trial phases I–IV.
  • Develop and validate programs for data analysis and reporting.
  • Prepare reports for regulatory submissions, publications, and internal reviews.
  • Provide statistical guidance across the trial lifecycle from protocol to close-out.
  • Contribute to protocol design and TNLD for trials and CSR tables/figures.
  • Collaborate with data management to ensure data quality and integrity.
  • Stay updated on statistical methodologies in clinical trials.

Skills

SAS
R
Biostatistics
Data analysis
Clinical trials

Education

MSc/PhD in Statistics/Biostatistics

Tools

CDISC SDTM/ADaM

Job description

Placements24 is seeking a Biostatistician to join a remote team in South Africa. The role focuses on designing, analyzing, and interpreting clinical trial data using SAS or R, contributing to regulatory submissions and publications.

The ideal candidate holds a MSc/PhD in Statistics or Biostatistics with at least 4 years in biostatistics within pharma/biotech, and a solid grasp of CDISC SDTM/ADaM. Remote work from anywhere in South Africa is offered.

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