Job Title: Senior Biostatistician
Location: Bangalore, India | India Remote
Job Type: Full Time
Date Posted: Posted Yesterday
Job Requisition ID: R15931
Company Overview:
At Clario, we are united in our commitment to transform clinical trials and improve lives through cutting-edge technology. We are expanding our Biostatistical team in India and offering an exciting opportunity for a Senior Biostatistician to join us on this journey. With a clear vision for the future, this is the perfect time to become part of our growing team.
What We Offer:
Competitive Compensation with shift allowances
Attractive Benefits including security, flexibility, support, and well-being
Engaging Employee Programs for continuous growth
Technology for Hybrid Working and great onsite facilities
Key Responsibilities & Authorities:
Statistical Analysis & Programming:
Create, test, and maintain SAS codes for statistical analysis related to cardiac safety.
Develop, test, and execute SAS and R programs for statistical analysis, including central tendency analysis, categorical analysis, and concentration-QTc analysis.
Validate results through double programming.
Deliverables & Documentation:
Prepare tables, figures, and listings for statistical analysis as per the Statistical Analysis Plan (SAP).
Perform quality checks on CDISC formatted analysis datasets (ADaM).
Review final outputs and reports based on the planned statistical analysis.
Support & Collaboration:
Support research programs and provide statistical insights to senior team resources and management.
Train team members on standard operating procedures and methodologies.
Work with cross-functional teams to ensure accurate scope of work for statistical deliverables.
Process Improvement & Supervision:
Develop and implement process improvements to increase operational efficiency.
Assist in creating and enforcing SOPs, SWIs, and templates for team deliverables.
Provide guidance and support to junior staff and ensure compliance with quality standards.
Client Interaction & Reporting:
Participate in client discussions to explain statistical methodologies and analysis techniques.
Manage timelines and ensure on-time delivery of projects.
Actively contribute to the hiring process and strategy development for the team.
What We’re Looking For:
Qualifications:
PhD in Statistics, Mathematics, or equivalent; or a Master’s degree with 4+ years of relevant experience; or Bachelor’s degree with 10+ years of relevant industry experience.
Skills & Experience:
Proficiency in SAS and R programming.
Familiarity with statistical methods such as ANOVA, t-test, regression, and linear mixed-effects modeling.
Experience in clinical trials within a CRO or pharmaceutical research organization.
Strong knowledge of CDISC SDTM and ADaM standards.
Familiarity with TFL generation and the pharmaceutical drug development process.
Additional Attributes:
Excellent verbal and written communication skills.
Strong organizational and analytical skills.
Ability to work independently and manage increasing responsibilities.
Ability to adapt to rapidly changing priorities.
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