About the Role
We are seeking a Biostatistician I to provide statistical expertise in the design, analysis, and interpretation of clinical studies. This role supports project teams across multiple phases of drug development, ensuring that statistical methodologies are appropriately applied and that study results are accurately reported. The Biostatistician collaborates closely with cross-functional teams including clinical, data management, and programming, and may contribute to regulatory submissions and publications.
Requirements
Experience:
1-3 years of experience.
Pharmaceutical, CRO, or related industry experience with clinical trials.
Technical Skills: Proficient in SAS and/or R; familiar with CDISC standards.
Education: Bachelor’s degree or master’s degree (or final-year student) in Biostatistics, Statistics, or a related field.
Knowledge: Understanding of ICH/GCP, Phase I–III trials.
Soft Skills: Good communication, teamwork.
Qualification
Strong understanding of clinical trial design and regulatory requirements.
Experience with clinical trial data management systems and clinical data standards.
Proficiency in statistical software and data management tools.
Responsibilities
Design, implement, and analyze clinical trial data using advanced statistical techniques.
Develop and validate statistical models to interpret complex datasets and inform study designs.
Collaborate with clinical and regulatory teams to ensure compliance with statistical standards and guidelines.