Senior Biostatistician - Clinical Trials

Placements24; Rustenburg; Hybrid; ZAR 900,000 - 1,200,000; Full time

Benefits offered by this job

Annual bonus

Health insurance

Retirement plan

Professional development

Job summary

Placements24 is seeking a Senior Biostatistician for its Clinical Trials unit in Rustenburg. You will design, analyze, and report on clinical studies, applying statistical methods and ensuring data integrity throughout the trial lifecycle.

You will collaborate with researchers, data managers, and regulators, perform SAS/R analyses, develop SAPs, and contribute to regulatory submissions and publications. A strong biostatistics background and excellent communication are essential.

Qualifications

• Master's or PhD in Biostatistics, Statistics, or related field.
• Minimum 6 years of biostatistics experience focused on clinical trial analysis.
• Proficiency in SAS and R.
• Strong understanding of regulatory requirements for clinical trials.
• Excellent communication and collaboration skills.
• Experience with data management is a plus.

Responsibilities

• Design protocols, sample size calculations, and SAPs.
• Perform complex statistical analyses of trial data using SAS or R.
• Interpret results and prepare reports for regulatory submissions.
• Collaborate with investigators to ensure accurate data collection.
• Provide statistical consultation throughout the study.
• Ensure adherence to GCP and regulatory guidelines.

Skills

Biostatistics

Study design

Regulatory knowledge

Communication skills

Education

Master's or PhD in Biostatistics

Tools

SAS

R

Job description

About the Role

Our client is seeking a highly skilled Senior Biostatistician to play a critical role in their Clinical Trials unit based in Rustenburg . This position is integral to the design, analysis, and reporting of clinical research studies, ensuring the integrity and validity of data. You will collaborate closely with clinical researchers, data managers, and regulatory experts to provide statistical expertise throughout the trial lifecycle. The ideal candidate possesses a strong quantitative background, extensive experience with statistical software, and a deep understanding of clinical trial methodologies. This role offers the chance to contribute to significant medical advancements and work within a supportive team dedicated to advancing patient care through rigorous scientific research in Rustenburg .

Key Responsibilities

• Design clinical trial protocols, sample size calculations, and statistical analysis plans.
• Perform complex statistical analyses of clinical trial data using SAS, R, or similar software.
• Interpret study results and prepare statistical reports for regulatory submissions and publications.
• Collaborate with investigators to ensure accurate data collection and study conduct.
• Provide statistical consultation and support to research teams throughout the study duration.
• Ensure adherence to Good Clinical Practice (GCP) and relevant regulatory guidelines.

Requirements

• Master's or PhD degree in Biostatistics, Statistics, or a related quantitative field.
• Minimum of 6 years of experience in biostatistics, with a significant focus on clinical trial analysis .
• Proficiency in statistical programming languages such as SAS and R.
• Strong understanding of statistical principles, study design, and regulatory requirements for clinical trials.
• Excellent communication and interpersonal skills, with the ability to explain complex statistical concepts clearly.
• Experience with data management and database querying is a plus.

Benefits

• An excellent annual salary with annual reviews and potential bonuses.
• Comprehensive health, dental, and vision insurance.
• Retirement savings plan with company contributions.
• Opportunities for continued professional development and advanced training.
• A dynamic and collaborative work environment in Rustenburg .
• The chance to contribute to life-changing medical research and development.