Biostatistician
Lexitas Pharma Services · United States · US
Clinical Data Science
Remote
Not yet analysed
Demand80
Career growth75
Healthcare fit60
Remote potential60
Salary band
USD 115k – 130k
5-year outlook
Biostatistician roles in CRO and pharma settings generally offer stable demand and compensation growth with seniority, statistical programming depth, and leadership experience. Exact salary depends on location, degree level, and prior clinical research experience.
Clinical license
Not required
Applicant reach
moderate
Seniority
entry
Employment type
full-time
Date found
2026-10-03
Intelligence details
Flexible work details
- Engagement type
- Contract
- Hours
- Variable hours
- Eligible countries
- United States
- Rate period
- Annual
Why this was classified this way
- contract
Listing via Himalayas.
Eligibility, licensing, and location restrictions can change. Always confirm details on the source posting before applying.
Why this is worth applying to
Worth applying for clinicians with strong quantitative, statistical, or clinical research backgrounds who want a non-clinical career in clinical trials. Less suitable for clinicians without statistics/programming training or interest in ophthalmology.
Who should apply
Physicians, pharmacists, IMGs, and healthcare graduates with biostatistics/statistics coursework or clinical research experience, especially those interested in ophthalmology, CROs, or pharma data roles.
CV angle
Highlight formal statistics/biostatistics training, clinical research experience, data analysis, programming (e.g., SAS/R), protocol/SAP/CSR contributions, cross-functional collaboration, and any ophthalmology or trial data exposure. Frame clinical background as domain expertise for interpreting endpoints and communicating with stakeholders.
Skills to highlight
- Biostatistics
- Statistical Analysis
- Clinical Trial Design
- SAS/R Programming
- Data Management
- Regulatory Submissions
- Cross-functional Collaboration
- Protocol/SAP/CSR Authoring
Role summary
Biostatistician supporting ophthalmic clinical trials by informing study design, analyzing and reporting trial data, authoring protocols/SAPs/CSRs, collaborating with data management and sponsors, and ensuring statistical integrity.
We publish our own intelligence summary, never the full job description. Always confirm details with the employer when you apply.