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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 recordThe US Department of Labor certified 7 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.
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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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✓
What Beam Therapeutics INC paid sponsored hires in similar roles2 certified filings for “Senior Director, Regulatory Affairs” (Regulatory Affairs Managers) in MA: $223k–$223k, median $223k.
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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
- The US Department of Labor certified 7 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. Source: LCA disclosure data (US Department of Labor (OFLC)).
- 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.
- What Beam Therapeutics INC paid sponsored hires in similar roles
- 2 certified filings for “Senior Director, Regulatory Affairs” (Regulatory Affairs Managers) in MA: $223k–$223k, median $223k. Most were filed at wage level IV (100%) — 4 lottery entries, ≈61% projected selection odds for cap-subject employers. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
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
Company Overview:
Beam Therapeutics is a biotechnology company committed to establishing the leading, fully integrated platform for precision genetic medicines. To achieve this vision, Beam has assembled a platform with integrated gene editing, delivery and internal manufacturing capabilities. Beam’s suite of gene editing technologies is anchored by base editing, a proprietary technology that is designed to enable precise, predictable and efficient single base changes, at targeted genomic sequences, without making double-stranded breaks in the DNA. This has the potential to enable a wide range of therapeutic editing strategies that Beam is using to advance a diversified portfolio of base editing programs. Beam is a values-driven organization committed to its people, cutting-edge science, and a vision of providing life-long cures to patients suffering from serious diseases.
Position Overview:
Beam is looking for a highly motivated, strategic, and collaborative leader to join our growing Commercial team. The Director will optimize patient delivery of risto-cel to Treatment Centers (TCs) with expertise in Sickle Cell Disease (SCD) and cell therapies. In collaboration with Quality, Supply Chain / Tech Ops, will ensure turnaround time, consistency in drug product delivery, and status update communications among other responsibilities. The Director will collaborate cross-functionally to define the strategy and operational oversight of the end-to-end patient and product journey from patient enrollment through treatment spanning the Beamlink portal, case management and commercial logistics.
This is an internal and external-facing role that requires close coordination with internal and external cross functional stakeholders to achieve successful results. Will be accountable for creating awareness regarding which patient delivery metrics are most relevant for a positive patient and treatment center experience. Work with the cross-functional team to set targets for patient delivery metrics and drive progress toward achievement of these goals. In preparation for commercialization this role will develop the team structure for the case management model and framework . This internal Beam single point of contact for the field facing team will streamline communication with the cross functional Beam team to meet the needs of the external facing teams to achieve business goals.
Responsibilities:
• Lead and develop a team of Case Managers and Logistics Managers.
• Support the development, testing, and implementation for business requirements of the Beamlink portal.
• Works with cross-functional Beam team (e.g., Technical Operations, Quality) to set targets for operational product delivery metrics and to drive product and process optimization to execute toward commercial targets.
• Assist in developing and executing integrated launch readiness plans with Commercial.
• Support treatment center account onboarding and activation.
• Develop the cell therapy cold-chain logistics, courier and vendor management processes.
• Define milestone communications, handoffs and escalation controls.
• Establish governance, operational controls and escalation pathway.
• Connect internal partners to resolve barriers in real time.
• Anticipate failure modes and put response mechanisms in place before launch.
Qualifications:
• BS/BA in a relevant academic field; MBA, MD, PhD, or other graduate degree strongly preferred.
• Typically 12 years of experience with 10 years business experience within the pharma/biotech/biopharma space.
• Experience in gene and/or cell therapy strongly desired, particularly in autologous cell therapy.
• Sophisticated understanding of the operational complexity and evolving scientific, clinical, regulatory, competitive, and ec
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