Physician Relations Jobs in USA with Visa Sponsorship
Physician Relations roles focus on building and maintaining partn visaerships between healthcare organizations and medical staff. Employers commonly sponsor H-1B visa and TN visas for qualified candidates with a bachelor's or master's degree in healthcare administration, business, or a related field. For detailed occupation requirements, see the O*NET profile.
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Senior Director Clinical Safety MD
Job Requisition ID:
1964
Posting Start Date:
8/4/26
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 Sr. Director, Clinical Safety, will lead the development and implementation of integrated project/product risk management strategies aimed at achieving the optimum benefit-risk for Development Sankyo's development compounds through the Safety Management Team framework. This individual will use strong leadership and communication skills to successfully coordinate resources and ensure effective collaboration across development functions and sites. The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle of the drug. Specific responsibilities will vary depending on the stage of development of assigned projects (i.e., Phase I through commercialization).
Responsibilities
- Depending on the status of development of the compound, lead and medical-scientifically direct a team of physicians and scientists responsible for a compound/product including project-specific training and coaching of team members and review of team output cross-functionally.
- Effectively represent the CSPV on the Global Product Team or other cross-functional teams providing the safety leadership and serving as the primary point of contact.
- Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals.
- Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management of assigned projects/products.
- Define and implement strategies and action plans for identifying and managing risks throughout the product life cycle.
- Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time.
- Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments).
Qualifications
Education Qualifications
MD Board certification or eligibility required
Experience Qualifications
6 or more years of experience in the pharmaceutical industry, regulatory agency or academia, with exposure to drug development, clinical pharmacology, and/or epidemiology is required
Experience in clinical development, submission and post marketing, is strongly recommended.
Physical Requirements
N/A N/A% of the time.
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$280,350.00 - USD$467,250.00
Download Our Benefits Summary PDF
Job Title:
Senior Director Clinical Safety MD
Job Requisition ID:
1964
Posting Start Date:
8/4/26
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 Sr. Director, Clinical Safety, will lead the development and implementation of integrated project/product risk management strategies aimed at achieving the optimum benefit-risk for Development Sankyo's development compounds through the Safety Management Team framework. This individual will use strong leadership and communication skills to successfully coordinate resources and ensure effective collaboration across development functions and sites. The individual assuming this role may function as a key member of the Global Product Team in collaboration with Clinical Development, Regulatory, Project Management, Biostatistics, Pharmacology, and other departments to strategically manage benefit-risk throughout the lifecycle of the drug. Specific responsibilities will vary depending on the stage of development of assigned projects (i.e., Phase I through commercialization).
Responsibilities
- Depending on the status of development of the compound, lead and medical-scientifically direct a team of physicians and scientists responsible for a compound/product including project-specific training and coaching of team members and review of team output cross-functionally.
- Effectively represent the CSPV on the Global Product Team or other cross-functional teams providing the safety leadership and serving as the primary point of contact.
- Review and analyze data from clinical trials, post-marketing and other relevant sources for the prompt identification of safety signals.
- Lead internal and external (especially regulatory, but also expert advisory) interactions to ensure quality outcomes in the risk evaluation and management of assigned projects/products.
- Define and implement strategies and action plans for identifying and managing risks throughout the product life cycle.
- Effectively coordinate and manage available resources in developing and delivering high-quality safety evaluation related documents/deliverables on time.
- Coordinate and participate actively in safety-related regulatory interactions (e.g., regulatory meetings, post-approval commitments).
Qualifications
Education Qualifications
MD Board certification or eligibility required
Experience Qualifications
6 or more years of experience in the pharmaceutical industry, regulatory agency or academia, with exposure to drug development, clinical pharmacology, and/or epidemiology is required
Experience in clinical development, submission and post marketing, is strongly recommended.
Physical Requirements
N/A N/A% of the time.
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$280,350.00 - USD$467,250.00
Download Our Benefits Summary PDF
See all 841+ Physician Relations Jobs
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Get Access To All JobsTips for Finding Physician Relations Jobs
Target health systems over private practices
Large hospital systems and integrated health networks have established immigration legal teams and sponsor visas routinely. Smaller private practices rarely have the infrastructure to manage H-1B or TN sponsorship, making them low-probability targets for international candidates.
Clarify the degree requirement upfront
Physician Relations roles must qualify as specialty occupations for H-1B sponsorship, meaning a specific bachelor's degree must be required, not merely preferred. Confirm the job posting states a degree requirement in a directly related field before investing time in the application.
Highlight relationship management metrics
Sponsoring employers want evidence of measurable impact. Quantify your experience with physician recruitment retention rates, partnership growth, or satisfaction scores. Concrete numbers strengthen both your candidacy and the employer's case for sponsorship approval with USCIS.
Canadian and Australian candidates explore TN and E-3
Canadian citizens in healthcare administration may qualify for TN status under the USMCA, bypassing the H-1B lottery entirely. Australian citizens should evaluate E-3 visa eligibility, which offers a dedicated annual allocation and no lottery requirement for specialty occupation roles.
Prepare for requests for evidence on specialty occupation
Physician Relations sits at the intersection of healthcare and administration, which USCIS occasionally scrutinizes. Ask your sponsoring employer's immigration counsel to document why the role requires specialized knowledge and a specific degree, reducing the risk of a Request for Evidence.
Engage hiring managers early on sponsorship willingness
Many health systems sponsor but do not advertise it explicitly. Raise visa sponsorship in the second or third interview once the employer has signaled genuine interest. Raising it too early can create friction before they have assessed your fit for the role.
Frequently Asked Questions
Can Physician Relations roles qualify for H-1B sponsorship?
Yes, but the role must meet the specialty occupation standard, meaning it requires at least a bachelor's degree in a specific field such as healthcare administration, business, or a closely related discipline. Generalist management positions where any degree suffices can be problematic. Roles at large health systems with documented degree requirements in the job description have the strongest foundation for H-1B visa approval.
What degree do I need to qualify for a sponsored Physician Relations position?
Most employers require a bachelor's degree in healthcare administration, business administration, public health, or a related field. Some senior roles specify a master's degree, particularly an MHA or MBA with a healthcare focus. If your degree is in an adjacent field, relevant work experience in physician engagement or hospital operations can strengthen the specialty occupation argument during H-1B adjudication.
How likely is USCIS to approve an H-1B petition for a Physician Relations role?
Approval rates are generally favorable when the employer documents a clear degree requirement and the applicant's credentials directly match. The main risk is a Request for Evidence questioning whether the role requires specialized knowledge beyond general business skills. Petitions from established health systems with detailed job descriptions and immigration-experienced legal counsel tend to clear adjudication without significant delays.
Where can I find Physician Relations jobs that offer visa sponsorship?
Migrate Mate filters job listings specifically by visa sponsorship eligibility, so you can browse Physician Relations openings without manually screening hundreds of postings. Health systems, academic medical centers, and large physician group practices are the most frequent sponsors. Searching by employer type rather than just job title on Migrate Mate can surface opportunities that generalist job boards miss entirely.
Can I work in Physician Relations on an OPT or STEM OPT extension while waiting for H-1B sponsorship?
Yes. If your degree is in a qualifying field, you can begin working under OPT immediately after graduation and transition to a STEM OPT extension if your degree falls under an eligible STEM classification, such as health informatics or business analytics. Your employer should file the H-1B petition during the spring registration window so the October 1 start date aligns with your OPT timeline. Plan at least six months ahead to avoid gaps in work authorization.
What is the prevailing wage requirement for sponsored Physician Relations jobs?
U.S. employers sponsoring a visa must pay at least the prevailing wage, which is what workers in the same role, area, and experience level typically earn. The Department of Labor sets this rate to make sure companies aren't hiring foreign workers simply because they'd accept lower pay than a U.S. worker. It varies by job title, location, and experience. You can look up current prevailing wage rates for any occupation and location using the OFLC Wage Search page.