About the Role
Our client, a prominent pharmaceutical research company, is seeking a skilled Biostatistician to join their data analytics team based in **East London, Eastern Cape**. This hybrid role offers flexibility, blending remote work capabilities with essential on-site collaboration for team synergy and data integrity. You will be responsible for the statistical design and analysis of clinical trials, contributing critical insights that support drug development and regulatory submissions. This is an excellent opportunity for a data-driven professional to apply advanced statistical methodologies in a dynamic pharmaceutical setting. The ideal candidate will possess strong analytical skills and a thorough understanding of clinical trial methodologies. You will play a key role in interpreting complex data sets, ensuring the robustness and reliability of our research findings, and ultimately contributing to the advancement of new therapies. Your expertise will be vital in shaping our understanding of clinical trial outcomes.
Key Responsibilities
- Design statistical analysis plans (SAPs) for clinical trials.
- Perform statistical analyses of clinical trial data using SAS, R, or other statistical software.
- Interpret statistical results and contribute to the preparation of clinical study reports (CSRs), publications, and presentations.
- Collaborate with clinical teams to ensure appropriate study design and data collection methods.
- Provide statistical input for protocols, case report forms (CRFs), and other study-related documents.
- Ensure adherence to statistical programming standards and regulatory guidelines.
- Contribute to the development of statistical methodologies and approaches.
- Perform exploratory data analyses and contribute to data review meetings.
- Stay updated on the latest advancements in statistical methodologies and software.
Requirements
- Master’s or Ph.D. in Statistics, Biostatistics, or a related quantitative field.
- Minimum of 3 years of experience as a Biostatistician in the pharmaceutical or biotech industry, with experience in clinical trial analysis.
- Proficiency in statistical software packages such as SAS, R, or similar.
- Strong understanding of statistical principles and methodologies relevant to clinical trials.
- Experience with survival analysis, longitudinal data analysis, and other relevant statistical techniques.
- Excellent analytical and problem-solving skills.
- Strong written and verbal communication skills, with the ability to explain complex statistical concepts clearly.
- Ability to work effectively both independently and as part of a hybrid team.
- Familiarity with CDISC standards is a plus.
Benefits
- Competitive salary and performance bonus.
- Comprehensive health, dental, and vision insurance.
- Retirement fund and savings plan.
- Generous annual leave and paid holidays.
- Hybrid work model providing work-life balance.
- Opportunities for professional development and continued learning.
Work within a collaborative and innovative research environment.
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