Senior Biostatistician - Clinical Trials

Placements24; Polokwane; Ibrido; ZAR 900.000 - 1.200.000; Tempo pieno

Vantaggi offerti da questo lavoro

Competitive salary

Hybrid work options

Professional development opportunities

Descrizione del lavoro

Placements24 in Polokwane invites an experienced Senior Biostatistician to lead the design and analysis of clinical trial data, ensuring robust interpretation and regulatory compliance.

You will collaborate with cross-functional teams, develop SAPs, perform SAS or R analyses, and contribute to study reports, with a focus on rigorous scientific methodology and impactful outcomes.

Competenze

• Master’s or Ph.D. in Biostatistics, Statistics, or related quantitative field.
• Minimum of 5 years in biostatistics within pharma/biotech, focused on clinical trials.
• Proficiency with SAS or R for analyses.
• Strong knowledge of clinical trial design and regulatory requirements (FDA/EMA).
• Excellent analytical and communication skills.
• Ability to work in a multidisciplinary team.

Mansioni

• Design statistical analysis plans for clinical trials, including sample size calculations.
• Perform statistical analyses using SAS or R; generate tables, listings, and figures.
• Interpret results and contribute to clinical study reports and regulatory submissions.
• Collaborate with cross‑functional teams to ensure scientifically sound study designs.
• Provide statistical guidance across drug development lifecycle.
• Stay updated on methodologies and regulatory guidelines.

Conoscenze

Biostatistics

Statistical analysis

Communication

Formazione

Master’s or Ph.D. in Biostatistics

Strumenti

SAS

R

Descrizione del lavoro

Our client is seeking an experienced Senior Biostatistician to join their leading clinical research team in Polokwane . This critical role involves the design, analysis, and interpretation of statistical data from clinical trials, ensuring the validity and integrity of research findings. You will collaborate closely with clinical researchers, data managers, and regulatory affairs specialists to support the development of new therapies. The ideal candidate possesses a deep understanding of statistical methodologies applicable to healthcare research and is committed to rigorous scientific inquiry, contributing to the successful progression of clinical development programs within a collaborative and impactful setting.

Key Responsibilities

• Design statistical analysis plans for clinical trials, including sample size calculations.
• Perform statistical analyses using SAS or R, generating tables, listings, and figures.
• Interpret statistical results and contribute to the preparation of clinical study reports and regulatory submissions.
• Collaborate with cross-functional teams to ensure study designs are statistically sound.
• Provide statistical expertise and guidance throughout the drug development lifecycle.
• Stay updated on statistical methodologies and regulatory guidelines relevant to clinical trials.

Requirements

• Master's or Ph.D. degree in Biostatistics, Statistics, or a related quantitative field.
• Minimum of 5 years of experience in biostatistics within the pharmaceutical or biotech industry, focusing on clinical trials.
• Proficiency in statistical analysis software such as SAS or R.
• Strong understanding of clinical trial design and regulatory requirements (e.g., FDA, EMA).
• Excellent analytical, problem-solving, and communication skills.
• Ability to work effectively in a multidisciplinary team environment.

Benefits

• Competitive salary and comprehensive benefits package.
• Opportunities for professional growth and development.
• Support for attending relevant statistical and clinical research conferences.
• Collaborative work environment focused on scientific rigor and innovation.
• Potential for hybrid work arrangements to support work-life balance.