Jobs / United States / Clinchoice INC
Senior Strategist - Regulatory Affairs (CMC)
Clinchoice INC · 🇺🇸 City, State/County - Country
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 roles1 certified filing for “Strategist, Regulatory Affairs” (Regulatory Affairs Specialists) in PA: $90k–$90k, median $90k. Most were filed at wage level III (100%) — 3 lottery entries, ≈46% 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
Responsibilities: • Manage the preparation and submission of new product registrations, post approval submission, and follow-up closely on queries and through approval • Responsible for reviewing and writing CMC modules 2 and 3 • Exposure to EU and CIS region in regulatory filings • Herbal product development background • Manage and coordinate product life cycle management • Ensure regulatory compliance with local regulatory requirements • Foster and maintain professional relationships with the health authorities • Provide regulatory support including timely registration of new product and line extensions to support new product launches and tender applications when necessary • Maintain regulatory work processes and tracking tools that improve performance levels and transparency • Exposure in writing of Product Quality Review • Promote regulatory intelligence in both local and regional initiatives • Develop regulatory strategies, prepare regulatory applications, and support maintenance activities within relevant therapy areas • Execution of regulatory strategies (local and regional) that are in line with the business plan • Complete regulatory activities for a defined number of products to ensure all regulatory obligations and business objectives are met • Ensure adherence to timelines and quality set parameters R • eview of formulation, generation of ingredient list, and claims per set standards • Compilation and review of labeling components per SOP Deliverables: • CMC modules 2 and 3 • Management of the preparation and submission of new product registrations, post approval submissions, and follow-up on queries through approval • Review of CMC modules • Execution of regulatory strategies (local and regional) that are in line with the business plan • Compilation of PQR as per SOP – Summary report of variations submitted as per the specified period. • Review of formulation, generation of ingredient list, and claims per set standards • Compilation and review of labeling components per SOP Experience/Qualifications: • Bachelor’s/Master’s degree in Life Science/Pharma • Six to eight years of relevant work experience • RAPS certification is desirable