About the Role
We are seeking an Associate Biostatistician 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:
Less than 0-1 year of relevant experience.
Pharmaceutical, CRO, or related industry experience with clinical trials.
Technical Skills: Basic SAS, R or Python; understanding of statistical concepts.
Education: Bachelor’s degree or master’s degree (or final-year student) in Biostatistics, Statistics, or a related field.
Knowledge: Basics of clinical trials and GCP.
Soft Skills: Willingness to learn, attention to detail.
Qualification
Basic knowledge of statistical methods and their applications in clinical research.
Experience in clinical trial data analysis or related internships.
Understanding of regulatory requirements in clinical research.
Responsibilities
Assist in the development of SAP and study protocols.
Perform data management and statistical analyses using software such as SAS or R.
Collaborate with cross-functional teams to ensure data integrity and compliance with regulatory standards.