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Sponsorship verdict
Sponsorship possible
One solid signal, not two. Worth applying, and worth asking about sponsorship early.
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Employer is on a government sponsor recordUSCIS Data Hub records 1 H-1B approvals for this employer in FY2023 — older 2023 data; no recent Department of Labor filings (Oct 2025 – Jun 2026) were found for it.
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The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
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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.
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Confirmed live todayWhen a source last listed this job as open.
Details and sources
- Employer is on a government sponsor record
- USCIS Data Hub records 1 H-1B approvals for this employer in FY2023 — older 2023 data; no recent Department of Labor filings (Oct 2025 – Jun 2026) were found for it. Source: US Department of Labor visa filings (LCA) (US Department of Labor (OFLC), plus USCIS H-1B Employer Data Hub).
- No salary bar for this route
- H-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.
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.
About the role
Medical Director - Neurology
Treeline has a robust research pipeline from discovery to clinic, and we are leveraging this for the greatest possible impact for patients. As a clinician and scientist, you will be bridging the basic research with clinical development strategy in this scientifically rich environment. This role will provide strategic medical guidance to lead the development of new neurology therapeutics and will be accountable for the design, implementation, and conduct of clinical development program(s) to support decision milestones and regulatory requirements.
Major Activities:
Clinical Development Planning
• Provide clinical leadership and strategic medical guidance for the development of new neurology therapeutics
• Responsible for creating clinical development plan(s) that foresee and support subsequent registration trials
• Maintain the highest standards of scientific and clinical knowledge.
• Stay informed and up to date of internal and external developments, trends, and other dynamics relevant to the clinical development plan, and maintain a current view of the disease area to inform strategy.
• Liaise with internal stakeholders and outside experts, advisory boards, patient advocacy groups and regulatory authorities and represent assigned programs to those groups and authorities
• May support Business Development and Licensing activities
Clinical Development Implementation
• Collaborate with clinical scientists, clinical operations, scientists and subject matter experts to develop clinical trial protocols
• Provide clinical and expert input in the development of clinical sections of Investigator Brochures, presentations, and other materials.
• Regularly engage with the relevant external investigators; participate in the identification and selection of appropriate external investigators and sites.
• Apply medical knowledge to guide the safe, ethical and efficient conduct of the trials under their responsibility
• Maintain compliance with Good Clinical Practice guidelines and Treeline Standard Operating Procedures
• Act as the medical monitor for assigned studies and conduct ongoing reviews of clinical trial data.
• Collaborate within a multidisciplinary team including biostatisticians, data managers and statistical programmers to develop study analytics and data review plans.
• Collaborate with the Translational Biomarker team to strategize, design, and implement biomarker plans.
• Review study data to ensure correct medical/scientific data interpretation for interim and final study reporting.
• Collaborate with Clinical Operations for site selection, feasibility, and query resolution etc.
• Collaborate with relevant team members to support regulatory interactions such as end of phase meetings.
Required Skills, Experience, and Education:
• MD with Board-certification (or equivalent expertise) with a neurology specialty. Clinical practice experience ≥ 4 years.
• Additional lab-based science training is required; PhD is preferred
• Experience leading complex, global, early phase clinical programs from the pharma/biotech industry and/or credible experience from an academic medical center
• Experience working with the principles and techniques of data analysis, interpretation, and clinical relevance.
• Excellent communication skills, written and oral
• Strong interpersonal skills
• Thorough knowledge of Good Clinical Practice
• Impeccable personal ethical integrity and a commitment to improving the outcomes for patients
This position is classified as exempt. The anticipated annual base salary range for candidates who will work in Watertown is $302,276 - $370,530. The final base salary offered to the successful candidate will be dependent upon several factors that may include but are n
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