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About the role
Key responsibilities & impact- Responsible for the design, analysis, and/or interpretation of clinical studies
- Act as the study lead for multiple studies, clinical programs, and/or large/complex studies
- Support the review and development of clinical programs
- May involve oversight of the statistical programming activities
- Ensure work is performed on time and of high quality
- Provide review and oversight to statistical output created by other members of the biostatistics department
Requirements
What you’ll need- Master’s degree (or Higher) in biostatistics, statistics, mathematics or other related disciplines
- General understanding and application of biostatistics in clinical trials
- Minimum of 6 years of related experience working in a Contract Research Organization
- Proficiency in one or more statistical programming language (SAS and R preferred)
Benefits
Comp & perks- Training and career development opportunities internally
- Strong emphasis on personal and professional growth
- Friendly, supportive working environment
- Opportunity to work with colleagues based all over the world, with English as the company language
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
BiostatisticsStatistical AnalysisStatistical ProgrammingData InterpretationClinical Study Design
Soft Skills
Quality AssuranceTime ManagementCollaboration
