Daiichi Sankyo Visa Sponsorship USA
Daiichi Sankyo is a global pharmaceutical and oncology company with a consistent track record of sponsoring international talent across research, clinical, and commercial functions. For skilled professionals in biotechnology and life sciences, it's a legitimate and active visa sponsor worth targeting in your U.S. job search.
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Get Access To All JobsJob Title:
Manager, Global Oncology HEOR & RWE
Job Requisition ID:
1243
Posting Start Date:
3/19/26
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
The Manager, Global Oncology HEOR & RWE will work cross-functionally to implement HEOR and RWE projects for the assigned assets under the direction of a Director or Sr. Director of Global Oncology HEOR & RWE. The person will work with clinical, market access, commercial, regional and medical affairs colleagues to support the clinical development and value creation of the company's oncology assets. Responsibilities include the implementation of outcomes research strategies, health economics research planning, and process improvements to ensure patient access to Daiichi Sankyo's products. This individual will ensure that rigorous HEOR studies are conducted to support the clinical and economic value proposition associated with the Daiichi Sankyo Oncology products. The work involves developing global cost effectiveness and budget impact models and to fill data gaps to support access needs, as well as to design and implement global outcomes research & health economic studies that supports key publications, reimbursement strategies. The person will work closely with other members of the Global Market Access & Pricing department to develop RWE and support market access initiatives aligned to Daiichi Sankyo's products, and represent the department in cross functional working groups and committees from time to time.
Responsibilities
HEOR and RWE Deliverables:
- Support the preparation of global value dossiers which present the product value propositions and the supporting evidence, aligned with the product development strategies and agreed/endorsed by the GPTs, GBTs, Regional HEOR and market access, to realize an optimal value demonstration of the products
- Conduct or support HEOR and RWE studies such as early economic models, burden of illness studies, external control arms to support single arm trials, and support the development and analysis of patient-reported outcomes (PRO) instruments in clinical trials
- Conduct literature reviews to build payer evidence, economic models, and Global Value Dossiers
- Support the analysis of clinical trial data for cost effectiveness models and market specific ad-hoc requests for reimbursement submissions
- Conduct RWE studies to support the value story for payers and reimbursement submissions
- Support the development of global cost effectiveness and budget impact models for HTA submissions to support reimbursement of indications for Daiichi Sankyo’s oncology products
- Develop HEOR and RWE communications (e.g. manuscripts, scientific forum presentations, slide decks, symposia), in collaboration with multi-functional teams, to build the peer reviewed published evidence supporting the value propositions for assigned products
- Manage vendors in the conduct of HEOR and RWE projects
Evidence Generation & Synthesis:
- Collaborate cross-functionally to gather overview information of target indications including epidemiology, disease burden, unmet needs, cost of illness, and treatment patterns/pathways
- Provide and maintain an in-depth understanding of changing Health Technology Assessments, Reimbursement & Access environment, payer requirements, and policies of key global markets
- Conduct evidence gap assessments in collaboration with global functions and key markets/regions
Stakeholder Engagement:
- Partner with Regional and Global stakeholders to assess and fill HEOR/RWE evidence gaps
- Collaborate with Clinical (R&D) to ensure that Payer and reimbursement requirements for key markets are included in the clinical trial / evidence generation plans
- Act as an ambassador to drive the access agenda with key stakeholders
Qualifications
Education Qualifications:
Bachelor's Degree in relevant discipline (e.g., health economics, medicine, pharmacy, public health, epidemiology) required
Experience Qualifications:
- 4 or more years overall relevant experience or commensurate education/experience required
- 1 or more years experience in HEOR field (in Healthcare, pharmaceuticals industry, or related) required
- Oncology experience, preferably with multi-indication compounds as well as with early-stage compounds
- Excellent understanding of the clinical development and life cycle of oncology medicines
- Strong knowledge of major markets and their PRA and HTA policies: US and Global (Europe required), both private and government setting
- Excellent understanding of HEOR and RWE concepts with hands on experience with HEOR methodologies across all phases of the product life cycle
- Track record of successful application of HEOR and RWE with key external stakeholders in major international markets
Travel Requirements
Ability to travel up to 30% of the time. Domestic and global travel
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$137,840.00 - USD$206,760.00
Job Title:
Manager, Global Oncology HEOR & RWE
Job Requisition ID:
1243
Posting Start Date:
3/19/26
At Daiichi Sankyo, we are united by a single purpose, to improve lives around the world through innovative medicines. With a legacy of innovation since 1899, a presence in more than 30 countries, and more than 19,000 employees, we are advancing breakthrough therapies in oncology, cardiovascular disease, rare diseases, and immune disorders. Guided by our 2030 vision to "be an innovative global healthcare company contributing to the sustainable development of society", we are shaping a healthier, more hopeful future for patients, their families, and society.
Job Summary
The Manager, Global Oncology HEOR & RWE will work cross-functionally to implement HEOR and RWE projects for the assigned assets under the direction of a Director or Sr. Director of Global Oncology HEOR & RWE. The person will work with clinical, market access, commercial, regional and medical affairs colleagues to support the clinical development and value creation of the company's oncology assets. Responsibilities include the implementation of outcomes research strategies, health economics research planning, and process improvements to ensure patient access to Daiichi Sankyo's products. This individual will ensure that rigorous HEOR studies are conducted to support the clinical and economic value proposition associated with the Daiichi Sankyo Oncology products. The work involves developing global cost effectiveness and budget impact models and to fill data gaps to support access needs, as well as to design and implement global outcomes research & health economic studies that supports key publications, reimbursement strategies. The person will work closely with other members of the Global Market Access & Pricing department to develop RWE and support market access initiatives aligned to Daiichi Sankyo's products, and represent the department in cross functional working groups and committees from time to time.
Responsibilities
HEOR and RWE Deliverables:
- Support the preparation of global value dossiers which present the product value propositions and the supporting evidence, aligned with the product development strategies and agreed/endorsed by the GPTs, GBTs, Regional HEOR and market access, to realize an optimal value demonstration of the products
- Conduct or support HEOR and RWE studies such as early economic models, burden of illness studies, external control arms to support single arm trials, and support the development and analysis of patient-reported outcomes (PRO) instruments in clinical trials
- Conduct literature reviews to build payer evidence, economic models, and Global Value Dossiers
- Support the analysis of clinical trial data for cost effectiveness models and market specific ad-hoc requests for reimbursement submissions
- Conduct RWE studies to support the value story for payers and reimbursement submissions
- Support the development of global cost effectiveness and budget impact models for HTA submissions to support reimbursement of indications for Daiichi Sankyo’s oncology products
- Develop HEOR and RWE communications (e.g. manuscripts, scientific forum presentations, slide decks, symposia), in collaboration with multi-functional teams, to build the peer reviewed published evidence supporting the value propositions for assigned products
- Manage vendors in the conduct of HEOR and RWE projects
Evidence Generation & Synthesis:
- Collaborate cross-functionally to gather overview information of target indications including epidemiology, disease burden, unmet needs, cost of illness, and treatment patterns/pathways
- Provide and maintain an in-depth understanding of changing Health Technology Assessments, Reimbursement & Access environment, payer requirements, and policies of key global markets
- Conduct evidence gap assessments in collaboration with global functions and key markets/regions
Stakeholder Engagement:
- Partner with Regional and Global stakeholders to assess and fill HEOR/RWE evidence gaps
- Collaborate with Clinical (R&D) to ensure that Payer and reimbursement requirements for key markets are included in the clinical trial / evidence generation plans
- Act as an ambassador to drive the access agenda with key stakeholders
Qualifications
Education Qualifications:
Bachelor's Degree in relevant discipline (e.g., health economics, medicine, pharmacy, public health, epidemiology) required
Experience Qualifications:
- 4 or more years overall relevant experience or commensurate education/experience required
- 1 or more years experience in HEOR field (in Healthcare, pharmaceuticals industry, or related) required
- Oncology experience, preferably with multi-indication compounds as well as with early-stage compounds
- Excellent understanding of the clinical development and life cycle of oncology medicines
- Strong knowledge of major markets and their PRA and HTA policies: US and Global (Europe required), both private and government setting
- Excellent understanding of HEOR and RWE concepts with hands on experience with HEOR methodologies across all phases of the product life cycle
- Track record of successful application of HEOR and RWE with key external stakeholders in major international markets
Travel Requirements
Ability to travel up to 30% of the time. Domestic and global travel
Daiichi Sankyo, Inc. is an equal opportunity/affirmative action employer. Qualified applicants will receive consideration for employment without regard to sex, gender identity, sexual orientation, race, color, religion, national origin, disability, protected veteran status, age, or any other characteristic protected by law.
Salary Range:
USD$137,840.00 - USD$206,760.00
Job Roles at Daiichi Sankyo Companies
How to Get Visa Sponsorship in Daiichi Sankyo Visa Sponsorship USA
Target roles in oncology and R&D first
Daiichi Sankyo's pipeline is heavily focused on oncology and antibody-drug conjugates. Clinical research, bioinformatics, and regulatory affairs roles in these areas are most likely to attract sponsorship, especially for candidates with specialized scientific backgrounds.
Apply early in the H-1B cycle
For H-1B sponsorship, Daiichi Sankyo typically files petitions in March for the October start date. Starting conversations with recruiters by January gives you the best chance of being included in that year's cap-subject filing window.
Research open roles with verified sponsorship history
Not every job posting from a pharmaceutical company includes sponsorship details. Migrate Mate surfaces verified sponsors so you can filter by real sponsorship history and focus only on Daiichi Sankyo roles confirmed to support international candidates.
Highlight regulatory or cross-border experience in your application
As a Japanese multinational operating in the U.S., Daiichi Sankyo values candidates who understand international regulatory frameworks like FDA and ICH guidelines. Emphasizing this experience signals immediate value and reduces the perceived cost of sponsorship.
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Get Access To All JobsFrequently Asked Questions
Does Daiichi Sankyo sponsor H-1B visas?
Yes, Daiichi Sankyo sponsors H-1B visas and has a consistent record of doing so across its U.S. operations. Sponsorship tends to be concentrated in technical and scientific roles within clinical development, regulatory affairs, and pharmaceutical research. If you're targeting an H-1B at Daiichi Sankyo, early engagement with recruiters before the March filing window is essential.
Which visa types does Daiichi Sankyo sponsor?
Daiichi Sankyo sponsors a range of visa types including H-1B, E-3, and TN visas, as well as F-1 OPT and CPT for students and recent graduates. The company also supports Green Card sponsorship through EB-2 and EB-3 pathways for longer-term employees, making it a viable option across multiple stages of an international career in the U.S.
Which departments or roles at Daiichi Sankyo are most likely to receive visa sponsorship?
Sponsorship at Daiichi Sankyo is most common in roles requiring specialized scientific or technical expertise. This includes clinical research and operations, regulatory affairs, biostatistics, pharmacovigilance, and oncology pipeline roles. Commercial and medical affairs positions may also attract sponsorship when the candidate profile is sufficiently specialized. Generalist or administrative roles are less likely to qualify.
How do I find open visa-sponsored jobs at Daiichi Sankyo?
The most reliable approach is to use Migrate Mate, which tracks verified sponsorship history by employer so you can see exactly which Daiichi Sankyo roles have supported international candidates. This saves time filtering through job listings that don't disclose sponsorship intent, and lets you focus your applications where they're most likely to succeed.
How do I time my application to Daiichi Sankyo for H-1B sponsorship?
H-1B petitions must be filed in March for an October 1 start date, so you need to have an offer in hand before that window opens. Aim to begin conversations with Daiichi Sankyo recruiters by December or January at the latest. For F-1 OPT holders already working in the U.S., the timeline is more flexible since cap-exempt filings can occur year-round in some circumstances.
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