Senior Biostatistician Consultant

Accountabilities

• Lead statistical activities for clinical trials, including study design, statistical analysis plan (SAP) development, and execution of analyses.
• Provide statistical expertise to cross-functional teams such as clinical operations, regulatory affairs, data management, and medical writing.
• Ensure accuracy and quality of statistical deliverables, including tables, listings, figures, and clinical study reports.
• Contribute to study protocols and CRF design to ensure appropriate statistical methodology is embedded from the outset.
• Develop, validate, and maintain SAS and/or R programming for clinical data analysis in compliance with SOPs and regulatory standards.
• Support process improvement initiatives to enhance statistical efficiency, consistency, and quality across projects.
• Provide mentorship and guidance to junior statisticians.

Requirements

• PhD or Master’s degree in Biostatistics or a related quantitative field.
• 3+ years of experience in biostatistics, ideally within clinical trials or consulting/outsourcing environments.
• Strong expertise in clinical trial design, sample size calculation, and statistical analysis.
• Proficiency in SAS and/or R programming.
• Solid knowledge of CDISC standards (SDTM, ADaM).
• Understanding of regulatory guidelines governing clinical trial analysis and reporting.
• Strong communication and collaboration skills in cross-functional environments.
• Ability to manage multiple projects and priorities in a fast-paced setting.

Benefits

• Competitive compensation aligned with experience
• Flexible work arrangements (remote/hybrid depending on project needs)
• Exposure to global clinical research programs across leading life sciences organizations
• Opportunity to work on innovative drug and medical device development projects
• Collaborative and expert-driven environment
• Continuous learning, mentorship, and career development opportunities
• Inclusive and diverse workplace culture

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