Daiichi Sankyo E-3 Visa Sponsorship Jobs USA
Daiichi Sankyo sponsors E-3 visas for Australian professionals in scientific and technical roles, particularly across oncology research, pharmaceutical development, and regulatory affairs. While not among the most prolific E-3 sponsors in the industry, the company does have an established pathway for qualified candidates in specialty occupation positions.
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Get Access To All JobsJob Title:
Associate Director GOMA Oncology Scientific Engagement
Job Requisition ID:
1446
Posting Start Date:
5/5/26
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 Associate Director, GMA Oncology, Scientific Engagement is responsible for the execution of activities in support of Global Medical Affairs Scientific Engagement strategies and plan for the Solid Tumor or Hematology therapeutic area (TA), under the guidance of the Director, GMA Oncology Scientific Engagement.
Responsibilities
- Execution of Global Key External Experts (KEE) engagement strategy and operational plan. Management and updating of KEE mapping and engagement plans, and related systems used for global coordination of medical activities.
-
Support coordination of Global scientific engagements (KEE, patient advocacy, professional society, and other HCP stakeholders) at major congresses, in collaboration with GMAT leads, regional and country medical leads, and other relevant internal cross-functional stakeholders. This includes alignment with Global Marketing, R&D, and Cancer Enterprise stakeholders.
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Support management of Vendor activities and tracking of milestones for payments of activities related to these GMA scientific engagement projects. Management of activities supported by grants & sponsorships, such as external medical education (CME, standalone or industry-sponsored symposia). Completion and submission of related legal and compliance applications and associated follow up with requestors. Responsible for the execution of global medical Advisory Boards and/or other input-seeking medical activities in alignment with GMAT lead.
-
Support management of Vendor activities and tracking of milestones for payments of activities related to GMA input-seeking projects. Manage consistent collection of medical insights from key global/regional/local medical activities for assigned TA in coordination with GMAT lead and other relevant cross-functional stakeholders and collate for reporting to key stakeholders and to help inform the overall medical plan for the respective TA. Support creation of standard operating procedures as it relates to Global Medical Affairs Scientific Engagement activities across the Oncology therapeutic area. Ensure all strategies, tactics, and activities are compliant with DS policies.
Qualifications
Education Qualifications
Bachelor's Degree required. A higher level degree such as a PhD, PharmD or Master's Degree in Health Sciences preferred.
Experience Qualifications
- Must have at least 7 years of professional experience (with a BS Degree) or 5 years with a doctorate degree, within the pharmaceutical industry at local, regional and/or Global level with PhD/PharmD.
-
Must have strong working knowledge of current clinical practice in Oncology / Hematology / Solid Tumor other relevant disease areas.
-
Have strong knowledge in and understanding of scientific engagement activities (including advisory boards, symposia).
-
Effectively engage external stakeholders across a broad range of audiences and activities.
-
Strong planning, coordination and organizational skills.
-
Strong influencing skills; Leads without authority.
-
Excellent project management skills.
-
Provide medical expertise to ensure successful product launches across functions.
-
Build strong internal and external relationships with diverse stakeholders that maximize alignment and organizational effectiveness.
-
Integrate medical expertise with commercial perspective.
-
Expertly manage ambiguity and complex situations.
Travel Requirements
Ability to travel up to 20% of the time both domestic & international.
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$162,400.00 - USD$243,600.00
Job Title:
Associate Director GOMA Oncology Scientific Engagement
Job Requisition ID:
1446
Posting Start Date:
5/5/26
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 Associate Director, GMA Oncology, Scientific Engagement is responsible for the execution of activities in support of Global Medical Affairs Scientific Engagement strategies and plan for the Solid Tumor or Hematology therapeutic area (TA), under the guidance of the Director, GMA Oncology Scientific Engagement.
Responsibilities
- Execution of Global Key External Experts (KEE) engagement strategy and operational plan. Management and updating of KEE mapping and engagement plans, and related systems used for global coordination of medical activities.
-
Support coordination of Global scientific engagements (KEE, patient advocacy, professional society, and other HCP stakeholders) at major congresses, in collaboration with GMAT leads, regional and country medical leads, and other relevant internal cross-functional stakeholders. This includes alignment with Global Marketing, R&D, and Cancer Enterprise stakeholders.
-
Support management of Vendor activities and tracking of milestones for payments of activities related to these GMA scientific engagement projects. Management of activities supported by grants & sponsorships, such as external medical education (CME, standalone or industry-sponsored symposia). Completion and submission of related legal and compliance applications and associated follow up with requestors. Responsible for the execution of global medical Advisory Boards and/or other input-seeking medical activities in alignment with GMAT lead.
-
Support management of Vendor activities and tracking of milestones for payments of activities related to GMA input-seeking projects. Manage consistent collection of medical insights from key global/regional/local medical activities for assigned TA in coordination with GMAT lead and other relevant cross-functional stakeholders and collate for reporting to key stakeholders and to help inform the overall medical plan for the respective TA. Support creation of standard operating procedures as it relates to Global Medical Affairs Scientific Engagement activities across the Oncology therapeutic area. Ensure all strategies, tactics, and activities are compliant with DS policies.
Qualifications
Education Qualifications
Bachelor's Degree required. A higher level degree such as a PhD, PharmD or Master's Degree in Health Sciences preferred.
Experience Qualifications
- Must have at least 7 years of professional experience (with a BS Degree) or 5 years with a doctorate degree, within the pharmaceutical industry at local, regional and/or Global level with PhD/PharmD.
-
Must have strong working knowledge of current clinical practice in Oncology / Hematology / Solid Tumor other relevant disease areas.
-
Have strong knowledge in and understanding of scientific engagement activities (including advisory boards, symposia).
-
Effectively engage external stakeholders across a broad range of audiences and activities.
-
Strong planning, coordination and organizational skills.
-
Strong influencing skills; Leads without authority.
-
Excellent project management skills.
-
Provide medical expertise to ensure successful product launches across functions.
-
Build strong internal and external relationships with diverse stakeholders that maximize alignment and organizational effectiveness.
-
Integrate medical expertise with commercial perspective.
-
Expertly manage ambiguity and complex situations.
Travel Requirements
Ability to travel up to 20% of the time both domestic & international.
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$162,400.00 - USD$243,600.00
Job Roles at Daiichi Sankyo
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Get Access To All JobsTips for Finding Daiichi Sankyo E-3 Visa Sponsorship Jobs USA
Align your degree to the role
Daiichi Sankyo's E-3 roles in drug development and regulatory affairs require a directly related degree, not just a science background. Check the O*NET occupation profile for your target role to confirm which degree fields satisfy the specialty occupation standard before applying.
Target oncology and regulatory teams first
Daiichi Sankyo's strongest hiring activity sits in oncology pipeline roles and regulatory submissions. Focusing your applications on these departments gives you the best shot at landing a role where the company already has a defined E-3 sponsorship process in place.
Confirm LCA filing before your offer letter
Your employer must file a certified Labor Condition Application with DOL before your E-3 application can proceed. When you receive an offer, ask your recruiter where the LCA process sits, since delays here push back your consulate appointment timeline.
Benchmark your salary against prevailing wage
Use the OFLC Wage Search to look up the prevailing wage for your specific job title and work location before negotiating your offer. Daiichi Sankyo must pay at least the prevailing wage on your LCA, so knowing that floor protects you and speeds up the filing.
Use Migrate Mate to handle your filing
Once you have a certified LCA and a signed offer letter, Migrate Mate can prepare and file your E-3 application for a flat fee. This is particularly useful if Daiichi Sankyo's HR team is less familiar with the E-3 process than with the H-1B visa.
Prepare for specialist credential questions at interview
Australian pharmacology and biotech degrees are generally accepted as U.S. equivalents, but consular officers at Sydney or Melbourne may ask how your specific credential maps to the role's requirements. Bring your official transcripts and, where applicable, a credential evaluation from a recognized assessment body.
Daiichi Sankyo E-3 Visa Sponsorship: Frequently Asked Questions
Does Daiichi Sankyo sponsor E-3 visas?
Yes, Daiichi Sankyo does sponsor E-3 visas for Australian nationals in qualifying specialty occupation roles. Sponsorship is most common in scientific, clinical, and regulatory functions where the role requires a directly related bachelor's degree or higher. You'll need a job offer and a certified LCA from the company before applying at a U.S. consulate in Australia.
Which roles at Daiichi Sankyo typically qualify for E-3 sponsorship?
E-3 sponsorship at Daiichi Sankyo is most common in oncology research, pharmaceutical sciences, regulatory affairs, clinical operations, and bioinformatics. These roles consistently meet the specialty occupation standard because they require a degree in a directly related scientific or technical field. Generalist or support roles without a specific degree requirement are less likely to qualify.
How do I start the E-3 application process at Daiichi Sankyo?
The process starts with a job offer, after which Daiichi Sankyo files a Labor Condition Application with DOL. Once the LCA is certified, you complete the DS-160 form, pay the MRV fee, and schedule a consulate interview in Australia. USCIS is not involved in a consular E-3 application, which means no petition filing and no lottery.
How long does the E-3 process take at Daiichi Sankyo?
LCA certification typically takes around seven business days. After that, consulate appointment wait times in Sydney and Melbourne vary by season and demand. Most applicants complete the full process, from offer to visa stamp in hand, within four to eight weeks. Starting early and confirming the LCA timeline with your Daiichi Sankyo HR contact helps avoid delays.
How do I find open E-3 jobs at Daiichi Sankyo?
Migrate Mate lists Daiichi Sankyo roles that have an active E-3 sponsorship history, filtered from DOL Labor Condition Application data. This lets you focus on positions where the company has already navigated the E-3 process rather than relying on job listings that don't specify visa support. Targeting roles in regulatory affairs and oncology gives you the strongest match with Daiichi Sankyo's known E-3 hiring patterns.
What is the prevailing wage for E-3 sponsorship at Daiichi Sankyo?
E-3 employers must pay at least the prevailing wage, determined when they file a Labor Condition Application with the Department of Labor. The rate is based on the role, location, and experience level, ensuring Australian hires are paid comparably to U.S. workers in the same position. You can look up prevailing wage rates for any occupation and location using the DOL's OFLC Wage Search tool.