Clinchoice Inc.
Statistical Programmer II/III (Permanent role)
United States · Mid
Stay score
odds of building a lasting career here
Thin sponsorship signal and lottery-bound. A low-probability bet with your clock running. Prioritize cap-exempt roles and proven entry-level sponsors first.
Lottery odds assume a STEM candidate.
Personalize to your clock →Employer immigration record
from this employer's Department of Labor filings
Green-card filing pattern in this occupation
Green-card follow-through: 90%
Sourced from Department of Labor LCA, PERM and prevailing-wage disclosure data. Employer matching is by name, so figures may be split across an employer's legal entities. Absence of a filing means none appears in our copy of the data, not that none exists.
Community outcomes
No reports yet — be the first to help the next applicant.
About the role
- We are seeking an experienced Statistical Programmer III with strong expertise in R programming to support clinical trial data analysis and reporting.
- The ideal candidate will have hands-on experience in developing, validating, and maintaining statistical outputs using R, along with a solid understanding of clinical data standards.
Responsibilities
- Develop, validate, and maintain statistical programs using SAS for the generation of Tables, Listings, and Figures (TLFs)
- Perform data manipulation, analysis, and visualization using R/SAS and relevant packages
- Collaborate with Biostatisticians and Data Management teams to support clinical study deliverables
Requirements
- Bachelor's or Master's degree in Statistics, Biostatistics, Computer Science, or a related field
- 3+ years of experience in statistical programming within the pharmaceutical/biotech industry
- Hands-on experience with R programming in a clinical trial environment
- Strong knowledge of clinical trial data and regulatory requirements
- Support submission activities and documentation as required
- Required Skills & Qualifications:
- Good understanding of R packages.
- Good understanding of CDISC standards (SDTM, ADaM)
Nice to have
- Experience working in an FSP model or with global pharmaceutical clients
- Exposure to submission activities (e.g., FDA/EMA)
- Familiarity with SAS alongside R is a plus
- Strong problem-solving and communication skills
- Once you have submitted your CV, you will receive an acknowledgement that we received it.
- If you have the requirements we need, you will be invited for phone interview as the first step.
- Unfortunately, due to the number of applications we receive, we cannot reply to everyone individually if you are not successful.
- Who will you be working for?
Visa & Work Authorization
- Are you interested in working directly for a single sponsor while having the security and additional career opportunities that working for a global CRO can bring?
This listing is sourced directly from Clinchoice Inc.'s careers page and normalized into a canonical job model.