Eikon Therapeutics Visa Sponsorship Jobs USA
Eikon Therapeutics is a pioneering biotech company developing novel therapeutics through cutting-edge single-molecule imaging technology. The company sponsors multiple visa types, including H-1B visa, E-3 visa, and Green Card pathways, making it a viable option for international scientists and researchers pursuing U.S. careers in drug discovery.
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Get Access To All JobsINTRODUCTION
Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
POSITION
We are seeking an experienced Director, Regulatory Affairs to support and execute regulatory strategy across our clinical-stage development programs. In this role, you will play a key role in both shaping regulatory strategy and driving hands-on execution across assigned programs. You will provide regulatory guidance throughout the development lifecycle, ensure alignment with FDA and international regulatory requirements, and partner closely with cross-functional teams to advance programs in a compliant, efficient, and high-quality manner. This role will report to a Senior Director, Regulatory Affairs, and requires a minimum of 3 days per week onsite (or more as business needs require) in our Jersey City, NJ, office to support effective cross-functional collaboration, operational excellence, and the evolving needs of our clinical development programs.
ABOUT YOU
You are a seasoned regulatory affairs professional with strong hands-on experience through clinical regulatory affairs content and strategy, and navigating FDA and international regulatory frameworks. You are comfortable operating as a senior individual contributor who leads programs through influence, partnership, and subject-matter expertise, rather than formal people management. You bring excellent communication, organizational, and problem-solving skills, and thrive in highly collaborative, fast-paced environments where you are expected to both think strategically and execute with rigor.
- Program-Focused Regulatory Leadership: Provide strategic and hands-on regulatory support across assigned clinical development programs, partnering closely with cross-functional teams to guide development and regulatory decision-making.
- Regulatory Strategy: Contribute to the development and execution of regulatory strategies supporting product development, approval, and commercialization in alignment with company objectives.
- Regulatory Compliance: Maintain current knowledge of evolving regulations, guidance, and industry best practices to ensure ongoing compliance across programs.
- Submission Management: Lead and/or support the preparation, review, and submission of regulatory documents, including INDs, NDAs, and MAAs, as applicable.
- Cross-Functional Collaboration: Work closely with Clinical Development, R&D, Quality, and other stakeholders to integrate regulatory considerations throughout the development lifecycle and drive alignment.
- Quality Support: Support regulatory aspects of quality systems, including compliance with GCP and GLP requirements.
- Risk Assessment: Identify regulatory risks, assess potential impact, and proactively recommend mitigation strategies.
QUALIFICATIONS
- Post-graduate degree with 10+ years of relevant regulatory affairs experience, or a Bachelor’s degree with 12+ years of experience.
- Strong working knowledge of FDA and international regulatory requirements (including regions such as EU, Japan, China) and guidelines.
- Demonstrated experience contributing to clinical regulatory content and strategy and managing regulatory submissions.
- Excellent written and verbal communication skills, with the ability to influence cross-functional stakeholders.
- Strong analytical skills, attention to detail, and sound judgment.
- Ability to thrive as an individual contributor in a dynamic, high-growth environment.
- Prior experience supporting oncology development programs is strongly preferred.
At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
- 401k plan with company matching
- Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
- Mental health and wellness benefits
- Weeklong summer and winter holiday shutdowns
- Generous paid time off and holiday policies
- Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
- Enhanced parental leave benefit
- Daily subsidized lunch program when on-site
The expected salary range for this role is $213,000 to $232,750 depending on skills, competency, and the market demand for your expertise.
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment. We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.
INTRODUCTION
Eikon Therapeutics is a new biopharmaceutical company employing revolutionary technology at the intersection of chemistry, engineering, computation, and biology to discover novel treatments for life-threatening diseases. Eikon’s discovery platform is built on groundbreaking innovations from its founders (Nobel Prize, 2014), culminating in the creation of microscopes which enable real time, molecular-resolution measurements of protein movement in living cells, thereby unlocking otherwise intractable classes of proteins as drug targets.
POSITION
We are seeking an experienced Director, Regulatory Affairs to support and execute regulatory strategy across our clinical-stage development programs. In this role, you will play a key role in both shaping regulatory strategy and driving hands-on execution across assigned programs. You will provide regulatory guidance throughout the development lifecycle, ensure alignment with FDA and international regulatory requirements, and partner closely with cross-functional teams to advance programs in a compliant, efficient, and high-quality manner. This role will report to a Senior Director, Regulatory Affairs, and requires a minimum of 3 days per week onsite (or more as business needs require) in our Jersey City, NJ, office to support effective cross-functional collaboration, operational excellence, and the evolving needs of our clinical development programs.
ABOUT YOU
You are a seasoned regulatory affairs professional with strong hands-on experience through clinical regulatory affairs content and strategy, and navigating FDA and international regulatory frameworks. You are comfortable operating as a senior individual contributor who leads programs through influence, partnership, and subject-matter expertise, rather than formal people management. You bring excellent communication, organizational, and problem-solving skills, and thrive in highly collaborative, fast-paced environments where you are expected to both think strategically and execute with rigor.
- Program-Focused Regulatory Leadership: Provide strategic and hands-on regulatory support across assigned clinical development programs, partnering closely with cross-functional teams to guide development and regulatory decision-making.
- Regulatory Strategy: Contribute to the development and execution of regulatory strategies supporting product development, approval, and commercialization in alignment with company objectives.
- Regulatory Compliance: Maintain current knowledge of evolving regulations, guidance, and industry best practices to ensure ongoing compliance across programs.
- Submission Management: Lead and/or support the preparation, review, and submission of regulatory documents, including INDs, NDAs, and MAAs, as applicable.
- Cross-Functional Collaboration: Work closely with Clinical Development, R&D, Quality, and other stakeholders to integrate regulatory considerations throughout the development lifecycle and drive alignment.
- Quality Support: Support regulatory aspects of quality systems, including compliance with GCP and GLP requirements.
- Risk Assessment: Identify regulatory risks, assess potential impact, and proactively recommend mitigation strategies.
QUALIFICATIONS
- Post-graduate degree with 10+ years of relevant regulatory affairs experience, or a Bachelor’s degree with 12+ years of experience.
- Strong working knowledge of FDA and international regulatory requirements (including regions such as EU, Japan, China) and guidelines.
- Demonstrated experience contributing to clinical regulatory content and strategy and managing regulatory submissions.
- Excellent written and verbal communication skills, with the ability to influence cross-functional stakeholders.
- Strong analytical skills, attention to detail, and sound judgment.
- Ability to thrive as an individual contributor in a dynamic, high-growth environment.
- Prior experience supporting oncology development programs is strongly preferred.
At Eikon, employee compensation also includes bonus and equity compensation, in addition to several generous benefit programs, including:
- 401k plan with company matching
- Medical (premiums covered by Eikon at 95%), dental and vision insurance (premiums covered by Eikon at 100%)
- Mental health and wellness benefits
- Weeklong summer and winter holiday shutdowns
- Generous paid time off and holiday policies
- Life/AD&D Insurance (premiums covered by Eikon at 100%) and optional supplemental employee-paid life/AD&D policies
- Enhanced parental leave benefit
- Daily subsidized lunch program when on-site
The expected salary range for this role is $213,000 to $232,750 depending on skills, competency, and the market demand for your expertise.
Eikon is proud to be an equal opportunity employer and will consider all qualified applicants for employment. We are currently not accepting any new third-party agencies or firms at this time. Please do not forward unsolicited agency resumes to our website, employees or Human Resources. Eikon Therapeutics will not pay fees to any third-party agency or firm associated with unsolicited resumes.
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Get Access To All JobsTips for Finding Eikon Therapeutics Visa Sponsorship Jobs USA
Target roles in research and drug discovery
Eikon Therapeutics's work in single-molecule imaging and therapeutics development means most sponsored roles sit in research, biology, chemistry, and engineering. Focus your application on positions where your scientific expertise directly aligns with their platform technology.
Understand which visa types they actually sponsor
Eikon sponsors H-1B, E-3, TN, F-1 OPT, and Green Card pathways. If you're Australian, the E-3 route can move significantly faster than H-1B. Knowing which visa fits your situation before applying strengthens your opening conversation with their recruiting team.
Lead with your scientific credentials upfront
Biotechnology employers like Eikon weigh advanced degrees heavily when evaluating visa sponsorship. Candidates with PhDs or master's degrees in relevant life sciences or engineering fields are far more likely to clear internal sponsorship approval thresholds during the hiring process.
Time your application around their hiring cycles
Biotech companies in early-to-growth stages like Eikon tend to hire in focused waves tied to funding and pipeline milestones. Monitor their open roles consistently rather than applying in one burst, Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history.
Ask about Green Card intentions during later interview stages
Eikon has sponsored both temporary and permanent residence pathways. If long-term U.S. stability matters to you, it's worth asking during offer discussions whether EB-2 or EB-3 sponsorship is part of their standard employment package for international hires in your role.
Prepare for a technically rigorous hiring process
Eikon Therapeutics hires at the frontier of biophysics and drug discovery, so expect deep technical screening regardless of your visa status. Demonstrating specific knowledge of their imaging platform or therapeutic focus areas will differentiate you from candidates with equivalent credentials on paper.
Frequently Asked Questions
Does Eikon Therapeutics sponsor H-1B visas?
Yes, Eikon Therapeutics sponsors H-1B visas. The company has an active track record of supporting international hires across its biotechnology and drug discovery teams. Roles requiring specialized scientific or engineering expertise are the most common candidates for H-1B sponsorship. If you're targeting Eikon, make sure your background aligns with their research platform before applying.
What visa types does Eikon Therapeutics sponsor?
Eikon Therapeutics sponsors several visa categories, including H-1B, E-3 visa, TN visa, F-1 OPT, and Green Card pathways through EB-2 or EB-3. This makes the company accessible to a range of international candidates, from Australian nationals who qualify for the E-3 visa to F-1 students finishing OPT. The right pathway depends on your nationality, degree, and role.
Which departments or roles at Eikon Therapeutics are most likely to receive visa sponsorship?
Given Eikon's focus on single-molecule imaging technology and therapeutic development, the roles most likely to attract visa sponsorship are in research science, computational biology, protein engineering, chemistry, and related technical functions. Positions requiring advanced degrees in life sciences or engineering are particularly well-suited for sponsorship approval within a biotech organization of this type.
How do I find open visa-sponsored jobs at Eikon Therapeutics?
Migrate Mate is the most direct way to find open roles at Eikon Therapeutics with confirmed visa sponsorship history. The platform verifies sponsorship track records so you're not guessing based on vague job descriptions. Filter by company name or visa type to see current openings that match your immigration situation and scientific background.
How do I approach the application process at Eikon Therapeutics as an international candidate?
Apply with your visa status clearly stated early, Eikon has sponsored international hires before, so it's not a red flag. Focus on demonstrating deep technical fit with their research areas, since biotech companies prioritize scientific alignment when deciding whether to sponsor. If you reach the offer stage, ask directly about their sponsorship process and typical timelines so you can plan accordingly.