Junior Statistician - (Permanent Role)

Summary

ClinChoice is a global full-service contract research organization supporting pharmaceutical, biotechnology, medical device, and consumer health companies. The Junior Statistician will support the planning, analysis, interpretation, and reporting of clinical trial data while collaborating with statisticians, programmers, data managers, and other cross-functional teams.

Responsibilities

• Support senior statisticians in the design and analysis of clinical studies
• Assist with statistical analysis plans (SAPs), table/listing/figure (TLF) specifications, and other statistical documentation
• Perform basic statistical analyses under appropriate guidance and supervision
• Support the review and interpretation of clinical trial data
• Assist with the preparation and review of statistical tables, listings, and figures
• Conduct data checks and identify discrepancies or potential data issues
• Support statistical programming activities and collaborate with statistical programmers
• Contribute to study reports, clinical study reports (CSRs), and other project documentation
• Maintain accurate and organized study documentation in accordance with project requirements and applicable guidelines
• Participate in project meetings and communicate progress, issues, and timelines effectively
• Follow company standard operating procedures (SOPs), project-specific procedures, and applicable regulatory requirements

Skills

• Bachelor's degree with relevant experience may also be considered
• 0–2 years of experience in statistics, biostatistics, or clinical research
• Basic understanding of statistical concepts and methodologies
• Good analytical, problem-solving, and organizational skills
• Strong attention to detail and ability to work effectively in a team environment
• Good written and verbal communication skills
• Master's degree in Statistics, Biostatistics, Mathematics, or a related quantitative discipline preferred
• Familiarity with clinical trial processes and pharmaceutical/biotech research is preferred
• Exposure to statistical software such as SAS, R, or Python is an advantage
• Exposure to clinical trial data and CDISC standards such as SDTM and ADaM
• Basic knowledge of clinical study design and statistical methods
• Experience working with statistical programming or clinical data is a plus

Qualifications

Must Haves

• Bachelor's degree with relevant experience may also be considered
• 0–2 years of experience in statistics, biostatistics, or clinical research
• Basic understanding of statistical concepts and methodologies
• Good analytical, problem-solving, and organizational skills
• Strong attention to detail and ability to work effectively in a team environment
• Good written and verbal communication skills

Nice to Haves

• Master's degree in Statistics, Biostatistics, Mathematics, or a related quantitative discipline preferred
• Familiarity with clinical trial processes and pharmaceutical/biotech research is preferred
• Exposure to statistical software such as SAS, R, or Python is an advantage
• Exposure to clinical trial data and CDISC standards such as SDTM and ADaM
• Basic knowledge of clinical study design and statistical methods
• Experience working with statistical programming or clinical data is a plus

Benefits

• Opportunity to work on global clinical research projects.
• Exposure to experienced statisticians and cross-functional teams.
• Opportunities for professional development and career growth.
• Collaborative and learning-oriented work environment.
• Continuous training to keep personnel qualified in terms of competence and expertise.
• Remote work