Junior Statistician / Biostatistician I
Locations: Bangalore and Chennai, India
Work Model: Office or Home (Hybrid/Remote Flexibility)
Employment Type: Full-Time
Job ID: JR143483
Application Deadline: February 17, 2026
Company: ICON plc
ThePharmaDaily.com is featuring an excellent opportunity for a Junior Statistician (Biostatistician I) with ICON plc, a globally recognized Clinical Research Organization (CRO) specializing in healthcare intelligence and clinical development services. This role is ideal for early-career biostatistics professionals with hands-on experience in statistical analysis within the pharmaceutical or clinical research industry.
Job Overview
The Junior Statistician will support clinical trial statistical activities, including study design input, statistical analysis planning, data review, and regulatory reporting. The role involves close collaboration with biostatisticians, statistical programmers, data management teams, and clinical stakeholders to ensure accurate, compliant, and high-quality statistical deliverables across clinical studies.
Key Responsibilities
Contribute to the design and statistical review of Case Report Forms (CRFs)
Review study database structures, edit checks, and coding conventions to ensure data integrity
Assist in preparing Statistical Analysis Plans (SAPs) including derivations, tables, listings, and figures (TLFs)
Perform statistical analyses using validated software tools
Interpret clinical data and communicate findings through clear statistical reports
Contribute to statistical sections of clinical study reports and integrated summaries
Collaborate with cross-functional teams to ensure timely and high-quality study deliverables
Support regulatory submission documentation as required
Required Qualifications and Experience
Master’s degree or higher in Statistics, Biostatistics, or a related quantitative field
Minimum 2+ years of experience in statistics or biostatistics within the pharmaceutical, biotech, or clinical research industry
Hands-on experience with R programming (mandatory)
Working knowledge of SAS and other statistical software packages
Strong understanding of clinical trial design, statistical methodologies, and regulatory requirements (ICH-GCP)
Familiarity with therapeutic area-specific statistical conventions preferred
Ability to translate clinical and client requirements into appropriate statistical methods
Excellent written and verbal communication skills
Strong interpersonal and project coordination skills
Core Competencies
Clinical trial statistical analysis
Statistical Analysis Plan (SAP) development
Data validation and integrity review
Regulatory submission support
Cross-functional collaboration and stakeholder communication
Compensation and Benefits
ICON offers a competitive compensation package aligned with industry standards, along with performance-based incentives. Employees receive country-specific benefits designed to support health, financial security, and work-life balance, which may include:
Annual leave entitlements
Health insurance coverage
Retirement planning programs
Life assurance
Global Employee Assistance Programme (TELUS Health)
Flexible optional benefits such as wellness initiatives and subsidized services
Equal Opportunity Statement
ICON is committed to building an inclusive and accessible workplace. All qualified applicants will receive equal consideration without discrimination based on protected characteristics. Reasonable accommodations are available during the recruitment and employment process where required.
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