Lead Biostatistician & Team Lead Clinical Trials (Cape Town)

Placements24; Cape Town; Vor Ort; ZAR 1.500.000 - 2.000.000; Vollzeit

Benefits dieser Stelle

Private medical insurance

Life assurance

Pension scheme

Zusammenfassung

Placements24 is seeking a senior Lead Biostatistician in Cape Town to lead the statistical design and analysis of clinical trials and to direct a team of biostatisticians. You will develop SAPs, oversee regulatory submissions, and collaborate with cross-functional teams to ensure high-quality statistical outputs.

The ideal candidate will have a Ph.D. or Master’s in Biostatistics, 10+ years in pharma, expertise in SAS and R, and a strong grasp of ICH/FDA/EMA guidelines.

Qualifikationen

• Ph.D. or Master’s in Biostatistics or related quantitative field from an accredited institution.
• Minimum of 10 years of experience in biostatistics within pharma/biotech.
• Proven leadership in statistical aspects of clinical trials from design to reporting.
• Expertise in SAS and R; proficient with statistical modeling.
• Strong understanding of regulatory guidelines (ICH, FDA, EMA).
• Excellent communication and leadership abilities.

Aufgaben

• Lead the design and analysis of clinical trials with regulatory rigor.
• Develop and implement SAPs for complex data sets.
• Mentor and manage a team of biostatisticians.
• Collaborate with clinical development, data management, and regulatory teams.
• Prepare and review CSRs, regulatory submissions, and publications.

Kenntnisse

SAS

R

Leadership

Communication

Project management

Ausbildung

Ph.D. or Master’s in Biostatistics

Tools

Statistical software

Jobbeschreibung

Placements24 is seeking a senior Lead Biostatistician in Cape Town to lead the statistical design and analysis of clinical trials and to direct a team of biostatisticians. You will develop SAPs, oversee regulatory submissions, and collaborate with cross-functional teams to ensure high-quality statistical outputs.

The ideal candidate will have a Ph.D. or Master’s in Biostatistics, 10+ years in pharma, expertise in SAS and R, and a strong grasp of ICH/FDA/EMA guidelines.