Junior Statistician - (Permanent Role- No Visa Sponsorship)
ClinChoice
•Remote
About The Position
ClinChoice is seeking a motivated and detail-oriented Junior Statistician to join their in-house team. This role will support statistical activities across clinical research projects, working closely with experienced statisticians, statistical programmers, data managers, and other cross-functional teams. The position involves supporting the planning, analysis, and reporting of clinical trial data for a diverse client portfolio including pharmaceutical, biotechnology, medical device, and consumer health companies.
Requirements
- Master's degree in Statistics, Biostatistics, Mathematics, or a related quantitative discipline preferred. 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.
- Familiarity with clinical trial processes and pharmaceutical/biotech research is preferred.
- Exposure to statistical software such as SAS, R, or Python is an advantage.
- 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
- 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.
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.
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.
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What This Job Offers
Job Type
Full-time
Career Level
Entry Level
