Taiho Oncology Visa Sponsorship USA
Taiho Oncology is a clinical-stage pharmaceutical company focused on cancer treatments, operating at the intersection of science and patient impact. For visa-sponsored roles in biotechnology and pharmaceuticals, Taiho Oncology has demonstrated a commitment to sponsoring permanent residency pathways for qualified candidates.
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Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients. It’s our work, our passion, and our legacy. We invite you to join us.
Hybrid
Employee Value Proposition:
This position provides an opportunity to build and implement the Medical Launch readiness plan for early pipeline products.
Position Summary:
The Medical Director, MA, must have strategic and scientific expertise, with an ability to sift thru specific clinical and disease state data. This individual has in depth understanding of pharmaceutical industry with strong business acumen and medical affairs launch experience to continually monitor changing market dynamics, market access and health care systems evolutions, metrics/insights that can impact the business side of the science. The Medical Director, MA must develop and implement launch readiness plan for assigned products. Ensure alignment and timely communications with internal matrix teams and external communications and exchange with key scientific leaders. Develop and refine tactics as needed, provide input into development and commercial plans. Requires a strong commitment to achieving corporate objectives while maintaining the highest ethical, regulatory, scientific standards and meaningful differentiation for medical practice adoption.
Performance Objectives:
- Lead the development of the Integrated Medical Affairs Plan (iMAP) and execute on medical affairs tactics that are aligned with the overall product development and Launch strategy.
- Provide active contributions into Target Product Profile (TPP), assessments of Patient Reported Outcomes (PROs) and Study Designs / End points.
- Strategically work cross functionally, partnering with other key functions at Taiho such as: Clinical Development, Commercial, HEOR, Market Access and Regulatory Affairs, Patient Advocacy, TOE, TPC and global teams to ensure as needed alignment and inputs.
- Develop Real world Evidence generation capability for building additional evidence for regulatory submission and post Launch assessments.
- Review investigator-sponsored study (IIST) proposals, Real world study protocols and collaborative research grants.
- Develop and facilitate MFT training Provide medical input and product expertise to develop Medical Communications, content and publication plan.
- Deliver scientific presentations to diverse audiences (e.g., physicians, pharmacists, marketing/medical agencies, and other key stakeholders) in investigator meetings, advisory and/or consulting settings.
- Partner with global thought leaders to provide insights on current focused early therapeutic areas unmet needs, gaps and questions from R&D colleagues.
Education/Certification Requirements:
MD is required.
Knowledge, Skills, and Abilities:
- Therapeutic Areas (TAs)- scientific training and experience in Oncology/Immunology required.
- A strong track record of success working in Medical Affairs, with at least 5 years of pharmaceutical industry experience in both HQ and field roles preferred.
- Strong sense of accountability, communication and presentation skills.
- Capability to work in a smaller and flatter organizational structure providing many diverse responsibilities, high visibility and access to Sr. Management.
- Ability to work effectively in a fast-paced and ever-changing environment.
- Proven track record of developing internal relationships and working effectively with cross-functional partners in a highly matrixed environment.
- A successful track record of developing project strategies and executing project details.
- Demonstrated ability in driving results to a positive outcome.
- Ability to engage in positive dialogues, influence outcomes and resolve conflicts in a constructive manner.
The pay range for this position at commencement of employment is expected to be between $271,150 - $319,000 annually. This pay range is based on the market range for positions of this type. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including annual bonus/incentive comp plans, potential long term incentive plan, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if a candidate/employee receives an offer of employment.
If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Location: Princeton, NJ #LI-Hybrid
Equal Opportunity Employer Information: Taiho Oncology is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, veteran status, gender identity, genetic information, or any other characteristic protected by federal, state, or local law. Any applicant who, because of a disability, needs an accommodation or assistance in completing an application or at any time during the application process, please email People@taihooncology.com. Taiho Oncology also provides reasonable accommodations to employees with disabilities consistent with our obligations under the law. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment qualified applicants with arrest and conviction records.
The incumbent in this position may be required to perform other duties, as assigned.

Looking for a chance to make a meaningful difference in the oncology space? Taiho Oncology is on a mission: to improve the lives of patients with cancer, their families, and caregivers. Our “People first” approach means we also highly value our employees, who work relentlessly to help execute our mission. Taiho’s success is founded on ensuring we always act with accountability, collaboration, and trust. By following these guiding principles, we earn and maintain the confidence of patients, the global healthcare community, collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types to address the ongoing and evolving needs of patients. Advanced technology, a world-class clinical development organization, and state-of-the-art facilities: these and other resources empower us to innovate and touch the lives of more and more patients. It’s our work, our passion, and our legacy. We invite you to join us.
Hybrid
Employee Value Proposition:
This position provides an opportunity to build and implement the Medical Launch readiness plan for early pipeline products.
Position Summary:
The Medical Director, MA, must have strategic and scientific expertise, with an ability to sift thru specific clinical and disease state data. This individual has in depth understanding of pharmaceutical industry with strong business acumen and medical affairs launch experience to continually monitor changing market dynamics, market access and health care systems evolutions, metrics/insights that can impact the business side of the science. The Medical Director, MA must develop and implement launch readiness plan for assigned products. Ensure alignment and timely communications with internal matrix teams and external communications and exchange with key scientific leaders. Develop and refine tactics as needed, provide input into development and commercial plans. Requires a strong commitment to achieving corporate objectives while maintaining the highest ethical, regulatory, scientific standards and meaningful differentiation for medical practice adoption.
Performance Objectives:
- Lead the development of the Integrated Medical Affairs Plan (iMAP) and execute on medical affairs tactics that are aligned with the overall product development and Launch strategy.
- Provide active contributions into Target Product Profile (TPP), assessments of Patient Reported Outcomes (PROs) and Study Designs / End points.
- Strategically work cross functionally, partnering with other key functions at Taiho such as: Clinical Development, Commercial, HEOR, Market Access and Regulatory Affairs, Patient Advocacy, TOE, TPC and global teams to ensure as needed alignment and inputs.
- Develop Real world Evidence generation capability for building additional evidence for regulatory submission and post Launch assessments.
- Review investigator-sponsored study (IIST) proposals, Real world study protocols and collaborative research grants.
- Develop and facilitate MFT training Provide medical input and product expertise to develop Medical Communications, content and publication plan.
- Deliver scientific presentations to diverse audiences (e.g., physicians, pharmacists, marketing/medical agencies, and other key stakeholders) in investigator meetings, advisory and/or consulting settings.
- Partner with global thought leaders to provide insights on current focused early therapeutic areas unmet needs, gaps and questions from R&D colleagues.
Education/Certification Requirements:
MD is required.
Knowledge, Skills, and Abilities:
- Therapeutic Areas (TAs)- scientific training and experience in Oncology/Immunology required.
- A strong track record of success working in Medical Affairs, with at least 5 years of pharmaceutical industry experience in both HQ and field roles preferred.
- Strong sense of accountability, communication and presentation skills.
- Capability to work in a smaller and flatter organizational structure providing many diverse responsibilities, high visibility and access to Sr. Management.
- Ability to work effectively in a fast-paced and ever-changing environment.
- Proven track record of developing internal relationships and working effectively with cross-functional partners in a highly matrixed environment.
- A successful track record of developing project strategies and executing project details.
- Demonstrated ability in driving results to a positive outcome.
- Ability to engage in positive dialogues, influence outcomes and resolve conflicts in a constructive manner.
The pay range for this position at commencement of employment is expected to be between $271,150 - $319,000 annually. This pay range is based on the market range for positions of this type. However, base pay offered may vary depending on multiple individualized factors, including market location, job-related knowledge, skills, and experience. The total compensation package for this position may also include other elements, including annual bonus/incentive comp plans, potential long term incentive plan, and discretionary awards in addition to a full range of medical, financial, and/or other benefits (including 401(k) eligibility and various paid time off benefits, such as vacation, sick time, and parental leave), dependent on the position offered. Details of participation in these benefit plans will be provided if a candidate/employee receives an offer of employment.
If hired, employee will be in an “at-will position” and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time, including for reasons related to individual performance, Company or individual department/team performance, and market factors.
Location: Princeton, NJ #LI-Hybrid
Equal Opportunity Employer Information: Taiho Oncology is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, gender, sex, age, religion, creed, national origin, ancestry, citizenship, marital status, sexual orientation, physical or mental disability, medical condition, veteran status, gender identity, genetic information, or any other characteristic protected by federal, state, or local law. Any applicant who, because of a disability, needs an accommodation or assistance in completing an application or at any time during the application process, please email People@taihooncology.com. Taiho Oncology also provides reasonable accommodations to employees with disabilities consistent with our obligations under the law. Pursuant to applicable state and municipal Fair Chance Laws and Ordinances, we will consider for employment qualified applicants with arrest and conviction records.
The incumbent in this position may be required to perform other duties, as assigned.
Job Roles at Taiho Oncology Companies
How to Get Visa Sponsorship in Taiho Oncology Visa Sponsorship USA
Target roles that align with Green Card pathways
Taiho Oncology's sponsorship history skews toward permanent residency rather than temporary work visas. Focus your application on clinical, regulatory, or research roles where long-term employment and Green Card sponsorship are more likely to be offered.
Highlight specialized oncology or pharmaceutical expertise
Taiho Oncology recruits highly specialized talent in cancer drug development. Candidates with backgrounds in oncology clinical trials, pharmacology, or regulatory affairs are better positioned to be considered for sponsored roles in a company this focused.
Understand EB-2 and EB-3 Green Card timelines before applying
Taiho Oncology sponsors EB-2 and EB-3 Green Cards. Knowing the difference, including priority date wait times based on your country of birth, will help you ask informed questions during interviews and set realistic expectations for the process.
Apply during active hiring cycles for scientific and regulatory teams
Biotechnology and pharmaceutical companies like Taiho Oncology tend to hire in cycles tied to clinical trial phases and regulatory milestones. Monitoring their careers page during product development announcements can surface sponsorship-eligible openings earlier.
Use Migrate Mate to find verified sponsorship-eligible roles
Not every job listing makes sponsorship status clear upfront. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history, making it easier to identify Taiho Oncology openings where visa support has been confirmed.
Come prepared to discuss your immigration situation directly
At a focused pharmaceutical company like Taiho Oncology, hiring decisions involve close coordination between HR and legal. Being transparent about your visa status and timeline during early conversations demonstrates professionalism and helps avoid delays later.
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Get Access To All JobsFrequently Asked Questions
Does Taiho Oncology sponsor H-1B visas?
Based on available sponsorship data, Taiho Oncology's visa support has been focused on Green Card sponsorship through the EB-2 and EB-3 categories rather than H-1B temporary work visas. If you're seeking H-1B sponsorship specifically, it's worth confirming directly with their HR team during the recruitment process, as sponsorship decisions can vary by role and timing.
What visa types does Taiho Oncology sponsor?
Taiho Oncology sponsors employment-based Green Cards, specifically through the EB-2 and EB-3 preference categories. EB-2 is typically used for roles requiring an advanced degree or exceptional ability, while EB-3 covers professionals and skilled workers. Both pathways require employer sponsorship and involve PERM labor certification before the immigrant petition is filed.
Which departments or roles at Taiho Oncology are most likely to receive visa sponsorship?
Taiho Oncology operates in oncology drug development, so sponsorship-eligible roles tend to sit within clinical development, regulatory affairs, medical affairs, and pharmaceutical sciences. These functions require specialized expertise that is often difficult to source domestically, making them more likely candidates for employer-sponsored Green Card filings.
How do I find open visa-sponsored jobs at Taiho Oncology?
The clearest way to find sponsorship-eligible openings at Taiho Oncology is through Migrate Mate, which surfaces verified sponsors and lets you filter roles by real sponsorship history rather than relying on job listings that may not disclose visa support. This saves time and helps you focus your applications on roles where sponsorship is confirmed.
How do I approach the application process at Taiho Oncology as a visa-sponsored candidate?
Start by identifying roles that match your scientific or regulatory background, since Taiho Oncology's sponsorship track record is concentrated in specialized pharmaceutical functions. Be upfront about your immigration status early in the process. Green Card sponsorship through EB-2 or EB-3 takes time, so aligning your timeline with the employer's expectations from the first conversation sets a stronger foundation.
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