Jobs / United States / Clinchoice INC
Senior Statistical Programmer/Analyst Consultant (Need solid oncology background) Remote in US
Clinchoice INC · 🇺🇸 United States
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 17 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 5 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Clinchoice INC paid sponsored hires in similar roles7 certified filings for “Senior Statistical Programmer/Analyst I” (Statisticians) in PA: $73k–$147k, median $82k. Most were filed at wage level I (57%) — 1 lottery entry, ≈15% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
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Sponsor Radar — Clinchoice INC
The US Department of Labor certified 17 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 5 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Clinchoice INC →
About the role
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? Our team says it’s the best of both worlds…. ClinChoice is searching for a Senior Statistical Programmer Consultant to join one of our clients. ClinChoice is a global full-service CRO with a strong focus on quality, professional development, and supportive culture. As a client-facing role, we are looking for confident candidates with the ability to work independently whilst establishing a high-trust environment with the client’s counterparts. We are seeking an experienced Senior Statistical Programmer with strong expertise in clinical trial programming and a solid background in oncology . The successful candidate will be capable of independently leading statistical programming activities across clinical studies, partnering closely with statisticians, clinical teams, and other cross-functional stakeholders. This role requires strong technical expertise in SAS programming, CDISC standards, and clinical trial reporting , along with the ability to take ownership of programming deliverables and provide guidance to junior team members. Key Responsibilities • Lead statistical programming activities for clinical studies within the oncology therapeutic area , from study start-up through database lock, analysis, and reporting. • Develop, review, and maintain high-quality SAS programs for SDTM, ADaM, Tables, Listings, and Figures (TLFs) . • Lead programming activities for interim and final analyses, including complex efficacy and safety analyses. • Work closely with Biostatisticians to understand statistical analysis plans, programming specifications, and study requirements. • Develop and review programming specifications and ensure consistency with study protocols, SAPs, and statistical methodology. • Support the creation and validation of CDISC-compliant SDTM and ADaM datasets . • Generate and validate TLFs for clinical study reports, regulatory submissions, and other clinical deliverables. • Perform independent programming validation and quality control of statistical outputs and datasets. • Support submission-related activities and respond to programming and data-related queries from cross-functional and regulatory teams. • Identify potential programming issues and proactively communicate risks, timelines, and solutions to project stakeholders. • Coordinate programming activities across studies and ensure deliverables are completed within agreed timelines and quality standards. • Provide technical guidance and mentorship to Statistical Programmers and other programming team members. • Participate in client/project meetings and effectively communicate technical information to both technical and non-technical stakeholders. Required Qualifications • Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field . • Strong experience in clinical trial statistical programming , preferably within a CRO, pharmaceutical, or biotechnology environment. • Significant experience working on oncology clinical trials . • Basic or working knowledge of R programming is preferred. • Experience supporting regulatory submissions • Strong proficiency in SAS programming , including Base SAS and relevant SAS procedures used for clinical trial reporting. • Strong knowledge of CDISC standards , particularly SDTM and ADaM. • Experience developing and validating TLFs for clinical trials. • Experience working with complex clinical trial data and supporting statistical analyses. • Ability to independently manage programming deliverables and lead study-level programming activities. • Strong understanding of clinical development pro