Jobs / United States / Clinchoice INC
Senior Statistical Programmer/Analyst Consultant (TA -Gene Therapy)-Remote
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 hands-on experience in Gene Therapy clinical trials to lead study-level statistical programming activities. The ideal candidate will have strong SAS programming expertise, a solid understanding of clinical trial data and regulatory requirements, and the ability to independently manage programming deliverables in collaboration with Biostatisticians and cross-functional teams. Experience in Gene Therapy clinical development is essential. Experience in Oncology or Internal Medicine is also valuable. Key Responsibilities • Lead statistical programming activities for Gene Therapy clinical trials from study start-up through database lock, analysis, and reporting. • Develop, review, and validate SAS programs for SDTM, ADaM, Tables, Listings, and Figures (TLFs). • Collaborate with Biostatisticians to interpret study protocols, Statistical Analysis Plans (SAPs), and programming specifications. • Develop and validate clinical datasets and statistical outputs for safety and efficacy analyses. • Support interim and final analyses, database lock activities, and Clinical Study Report preparation. • Ensure programming deliverables comply with CDISC standards and applicable regulatory requirements. • Perform independent validation and quality control of datasets, TLFs, and other programming outputs. • Support regulatory submissions and address programming-related questions from internal and external stakeholders. • Manage study-level programming timelines, deliverables, and quality expectations. • Identify and resolve complex programming issues and proactively communicate risks. • Provide technical guidance and mentorship to other Statistical Programmers. • Participate in client-facing meetings and collaborate with cross-functional project teams. Required Qualifications • Bachelor's or Master's degree in Statistics, Biostatistics, Mathematics, Computer Science, or a related field. • Significant experience in clinical trial statistical programming within a pharmaceutical, biotechnology, or CRO environment. • Hands-on experience supporting Gene Therapy clinical trials is required. • Strong proficiency in SAS programming. • Strong knowledge of CDISC standards, including SDTM and ADaM. • Experience developing and validating clinical trial TLFs. • Ability to independently lead study-level programming activities. • Understanding of clinical trial processes, statistical analysis, and regulatory reporting. • Excellent analytical, communication, and problem-solving skills. The Application Process 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? About ClinChoice ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of prove