Position Overview
Client is seeking a Sr. Biostatistician to support clinical trial design analysis and reporting within the Biostatistics & Statistical Modelling organization. The role contributes directly to compound/program development plans and Health Authority (HA) submissions while collaborating closely with cross-functional teams.
Key Responsibilities
- Provide statistical expertise in the design execution and analysis of one or more clinical trials.
- Partner with program stakeholders to ensure timely delivery of statistical deliverables.
- Support statistical input for regulatory submissions and clinical development plans.
- Oversee statistical processes across multiple trials ensuring compliance with company SOPs and regulatory requirements.
- Clearly communicate complex statistical concepts to non-statistical audiences.
- Act as a proactive contributor and project lead in cross-functional team settings.
Required Qualifications
- Masters degree in Statistics Biostatistics or related field (Ph.D. strongly preferred).
- Minimum 5 years of experience (doctoral research may count toward this requirement).
- Proven expertise in drug development and application of biostatistics to clinical trials.
- Proficiency in statistical software such as SAS and/or R.
- Experience planning supervising and monitoring statistical activities across multiple studies.
- Strong written and verbal communication skills in English.
- Ability to work independently while contributing effectively in a collaborative team environment.
Position Overview Client is seeking a Sr. Biostatistician to support clinical trial design analysis and reporting within the Biostatistics & Statistical Modelling organization. The role contributes directly to compound/program development plans and Health Authority (HA) submissions while collaborati...
Position Overview
Client is seeking a Sr. Biostatistician to support clinical trial design analysis and reporting within the Biostatistics & Statistical Modelling organization. The role contributes directly to compound/program development plans and Health Authority (HA) submissions while collaborating closely with cross-functional teams.
Key Responsibilities
- Provide statistical expertise in the design execution and analysis of one or more clinical trials.
- Partner with program stakeholders to ensure timely delivery of statistical deliverables.
- Support statistical input for regulatory submissions and clinical development plans.
- Oversee statistical processes across multiple trials ensuring compliance with company SOPs and regulatory requirements.
- Clearly communicate complex statistical concepts to non-statistical audiences.
- Act as a proactive contributor and project lead in cross-functional team settings.
Required Qualifications
- Masters degree in Statistics Biostatistics or related field (Ph.D. strongly preferred).
- Minimum 5 years of experience (doctoral research may count toward this requirement).
- Proven expertise in drug development and application of biostatistics to clinical trials.
- Proficiency in statistical software such as SAS and/or R.
- Experience planning supervising and monitoring statistical activities across multiple studies.
- Strong written and verbal communication skills in English.
- Ability to work independently while contributing effectively in a collaborative team environment.
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