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Senior Biostatistician

10+ years
Not Disclosed
10 April 16, 2025
Job Description
Job Type: Full Time Education: B.Sc./PhD/M.Sc./B.Pharm/M.Pharm/Life science Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

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.