Senior Clinical Research Scientist Jobs in USA with Visa Sponsorship
Senior Clinical Research Scientist roles qualify as H-1B visa specialty occupations, making them strong candidates for employer visa sponsorship. Pharmaceutical companies, CROs, and academic medical centers regularly file Labor Condition Applications for this title. An advanced degree in a life sciences discipline is typically required. For detailed occupation requirements, see the O*NET profile.
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Get Access To All JobsINTRODUCTION
Anteris® Technologies is a global structural heart company dedicated to revolutionizing cardiac care. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team. Our mission is to forge new frontiers in cardiac care by pioneering science-driven and measurable advancements to restore heart valve patients to healthy function. Transcatheter Aortic Valve Replacement (TAVR) technologies were originally designed for older, high-risk patients. Today, younger, more active patients need a better solution that will not just open and close but restore healthy heart function. We seek to restore healthy blood flow patterns by creating the world’s first biomimetic TAVR valve, DurAVR® THV. This cutting-edge valve, incorporating our proprietary ADAPT® anti-calcification technology, is designed to mimic the natural function of a healthy heart valve.
ROLE AND RESPONSIBILITIES
The Senior Clinical Research Scientist will provide scientific, clinical, and operational expertise to support Anteris’ global clinical studies and ensure scientific objectives are achieved. This individual will work cross-functionally on the design, execution, monitoring, interpretation, and communication of clinical trial data to help advance patient outcomes through Anteris’ breakthrough structural heart technologies. This position reports to the Senior Manager, Clinical Research and collaborates closely with the broader clinical and cross-functional teams to support ongoing clinical studies, clinical documentation, and the dissemination of clinical data through publications and congress activities. This is a highly visible role with the opportunity to make a significant impact at Anteris Technologies. At Anteris Technologies, you’ll join a mission-driven team dedicated to improving the lives of patients with aortic stenosis through breakthrough structural heart technologies while helping shape the future of structural heart care.
Primary Duties And Responsibilities
- Represent Anteris as an industry leader within scientific, clinical research, and industry organizations
- Serve as a Scientific Lead and Subject Matter Expert for Anteris-sponsored clinical studies
- Partner cross-functionally to support the scientific objectives of Anteris-sponsored clinical studies and advance the company’s mission as a science-driven organization
- Lead execution of the subject selection process to ensure accurate and timely review of subject eligibility criteria, with oversight from clinical leadership
- Oversee external vendor performance and drive effective cross-functional collaboration
- Contribute to clinical trial design, protocol development, protocol revisions, and reports supporting regulatory submissions, with guidance from clinical leadership
- Participate in publication planning activities in collaboration with cross-functional stakeholders
- Support charter development for clinical studies in partnership with external vendors and study leadership, with oversight from clinical leadership
- Perform data analysis and interpretation in collaboration with external biostatisticians and internal data management teams
- Deliver timely study updates to clinical and cross-functional leadership through clear, well-structured presentations and data summaries
- Develop, maintain, and review clinical study reports and related documentation
- Contribute to root cause analyses, corrective and preventive actions, and effectiveness monitoring, with oversight from clinical leadership
- Collaborate with internal and external stakeholders, including study sites, vendors, and committees, to support clinical trial objectives and appropriately escalate issues when needed
- Build and maintain strong relationships with study investigators and key opinion leaders
- Contribute to Medical Legal Review (MLR) activities as a clinical subject matter expert for external data releases, ensuring scientific accuracy and appropriate clinical interpretation prior to publication or disclosure
- Assist in compiling clinical documentation and data for regulatory submissions
- Provide cross-functional clinical training and education support
BASIC QUALIFICATIONS
- Advanced degree in Life Sciences required; MD or PhD preferred
- 5+ years of Clinical Science or Clinical Research experience within cardiology, cardiovascular, or medical device environments
- Experience contributing scientifically to medical device clinical trials
- Proficiency in medical terminology and medical writing, including experience working within ICMJE guidelines
- Knowledge of healthcare ethics and compliance regulations
- Strong work ethic, self-motivation, collaboration skills, and excellent written and verbal English communication skills
PREFERRED QUALIFICATIONS
- TAVR clinical research experience strongly preferred
- Extensive clinical or scientific experience with advanced training in research, study design, and statistics (MSN, PhD, MS, or equivalent)
- Experience with imaging modalities, including echocardiography, CT, and CMR interpretation
- Experience supporting international, multi-center, randomized clinical trials
- Experience with statistical software programs such as Matlab, SPSS, or SAS is a strong plus
WHAT WE OFFER
- Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.
- Collaborative and dynamic work environment with a culture of innovation and excellence.
- Competitive compensation package, including salary, performance-based bonuses, and stock options.
- Career development opportunities and a chance to be part of a growing company that values its employees.
HEALTH AND WELLNESS OFFERINGS
- Medical, Dental, and Vision Plans
- Flexible Spending Account (FSA)
- 401k + Company Match
- Life, AD&D, Short-Term and Long-Term Disability Insurance
- Bonus Plan Eligibility
- Employee Stock Option Plan
- Paid Holidays & Vacation
- Employee Assistance Program
- Inclusive Team Environment
COMPENSATION
Salary Range: $130,000 - $160,000 USD
Note: We may require proof of COVID-19 vaccination to comply with health institutions, state, local municipality, and/or travel regulations.
Anteris Technologies recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale.
INTRODUCTION
Anteris® Technologies is a global structural heart company dedicated to revolutionizing cardiac care. With offices in Minneapolis, MN, US; Geneva, Switzerland; and Brisbane and Perth, Australia, we have a growing and inclusive team. Our mission is to forge new frontiers in cardiac care by pioneering science-driven and measurable advancements to restore heart valve patients to healthy function. Transcatheter Aortic Valve Replacement (TAVR) technologies were originally designed for older, high-risk patients. Today, younger, more active patients need a better solution that will not just open and close but restore healthy heart function. We seek to restore healthy blood flow patterns by creating the world’s first biomimetic TAVR valve, DurAVR® THV. This cutting-edge valve, incorporating our proprietary ADAPT® anti-calcification technology, is designed to mimic the natural function of a healthy heart valve.
ROLE AND RESPONSIBILITIES
The Senior Clinical Research Scientist will provide scientific, clinical, and operational expertise to support Anteris’ global clinical studies and ensure scientific objectives are achieved. This individual will work cross-functionally on the design, execution, monitoring, interpretation, and communication of clinical trial data to help advance patient outcomes through Anteris’ breakthrough structural heart technologies. This position reports to the Senior Manager, Clinical Research and collaborates closely with the broader clinical and cross-functional teams to support ongoing clinical studies, clinical documentation, and the dissemination of clinical data through publications and congress activities. This is a highly visible role with the opportunity to make a significant impact at Anteris Technologies. At Anteris Technologies, you’ll join a mission-driven team dedicated to improving the lives of patients with aortic stenosis through breakthrough structural heart technologies while helping shape the future of structural heart care.
Primary Duties And Responsibilities
- Represent Anteris as an industry leader within scientific, clinical research, and industry organizations
- Serve as a Scientific Lead and Subject Matter Expert for Anteris-sponsored clinical studies
- Partner cross-functionally to support the scientific objectives of Anteris-sponsored clinical studies and advance the company’s mission as a science-driven organization
- Lead execution of the subject selection process to ensure accurate and timely review of subject eligibility criteria, with oversight from clinical leadership
- Oversee external vendor performance and drive effective cross-functional collaboration
- Contribute to clinical trial design, protocol development, protocol revisions, and reports supporting regulatory submissions, with guidance from clinical leadership
- Participate in publication planning activities in collaboration with cross-functional stakeholders
- Support charter development for clinical studies in partnership with external vendors and study leadership, with oversight from clinical leadership
- Perform data analysis and interpretation in collaboration with external biostatisticians and internal data management teams
- Deliver timely study updates to clinical and cross-functional leadership through clear, well-structured presentations and data summaries
- Develop, maintain, and review clinical study reports and related documentation
- Contribute to root cause analyses, corrective and preventive actions, and effectiveness monitoring, with oversight from clinical leadership
- Collaborate with internal and external stakeholders, including study sites, vendors, and committees, to support clinical trial objectives and appropriately escalate issues when needed
- Build and maintain strong relationships with study investigators and key opinion leaders
- Contribute to Medical Legal Review (MLR) activities as a clinical subject matter expert for external data releases, ensuring scientific accuracy and appropriate clinical interpretation prior to publication or disclosure
- Assist in compiling clinical documentation and data for regulatory submissions
- Provide cross-functional clinical training and education support
BASIC QUALIFICATIONS
- Advanced degree in Life Sciences required; MD or PhD preferred
- 5+ years of Clinical Science or Clinical Research experience within cardiology, cardiovascular, or medical device environments
- Experience contributing scientifically to medical device clinical trials
- Proficiency in medical terminology and medical writing, including experience working within ICMJE guidelines
- Knowledge of healthcare ethics and compliance regulations
- Strong work ethic, self-motivation, collaboration skills, and excellent written and verbal English communication skills
PREFERRED QUALIFICATIONS
- TAVR clinical research experience strongly preferred
- Extensive clinical or scientific experience with advanced training in research, study design, and statistics (MSN, PhD, MS, or equivalent)
- Experience with imaging modalities, including echocardiography, CT, and CMR interpretation
- Experience supporting international, multi-center, randomized clinical trials
- Experience with statistical software programs such as Matlab, SPSS, or SAS is a strong plus
WHAT WE OFFER
- Opportunity to make a significant impact on the healthcare industry by advancing groundbreaking therapies.
- Collaborative and dynamic work environment with a culture of innovation and excellence.
- Competitive compensation package, including salary, performance-based bonuses, and stock options.
- Career development opportunities and a chance to be part of a growing company that values its employees.
HEALTH AND WELLNESS OFFERINGS
- Medical, Dental, and Vision Plans
- Flexible Spending Account (FSA)
- 401k + Company Match
- Life, AD&D, Short-Term and Long-Term Disability Insurance
- Bonus Plan Eligibility
- Employee Stock Option Plan
- Paid Holidays & Vacation
- Employee Assistance Program
- Inclusive Team Environment
COMPENSATION
Salary Range: $130,000 - $160,000 USD
Note: We may require proof of COVID-19 vaccination to comply with health institutions, state, local municipality, and/or travel regulations.
Anteris Technologies recruits, employs, trains, compensates, and promotes regardless of race, religion, color, national origin, sex, disability, age, veteran status, and other protected status as required by applicable law. We have a clear vision: to be a place of belonging for all humans by promoting diversity, multiculturism and inclusion, as a goal and reflection across the organization. Diversity is more than a commitment - it is part of our mission to deliver the best structural heart products on a global scale.
See all 1,151+ Senior Clinical Research Scientist Jobs
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Get Access To All JobsTips for Finding Visa Sponsorship as a Senior Clinical Research Scientist
Align your degree to the role
H-1B eligibility for this role hinges on a direct connection between your degree field and clinical research. A degree in pharmacology, biostatistics, or a related life science strengthens your specialty occupation case far more than a general biology degree.
Target CROs and pharma sponsors strategically
Contract research organizations and large pharmaceutical companies file the most LCAs for clinical research scientist titles. Prioritize employers with active IND portfolios or Phase II and III trial pipelines, as those operations create sustained demand for mid-to-senior research staff.
Verify prevailing wage before negotiating
Your employer must certify your wage meets DOL prevailing wage levels on the LCA. Use the OFLC Wage Search to look up the Level III or Level IV wage for your metro area before you enter salary discussions, so you're not caught off guard.
Search verified sponsoring employers on Migrate Mate
Filter your job search to employers with confirmed LCA filing history for clinical research roles. Migrate Mate surfaces employers with verified DOL sponsorship records, so you spend time on roles with real sponsorship intent rather than guessing from job descriptions.
Prepare your credential documentation early
Foreign life sciences degrees often require a credential evaluation for USCIS specialty occupation review. Get a detailed course-by-course evaluation from a NACES-member evaluator before your employer files, not after, to avoid delays from a Request for Evidence.
Understand the LCA filing timeline relative to your start date
Your employer must file a certified LCA with DOL before submitting the H-1B petition to USCIS. DOL certification typically takes seven business days, so factor that into onboarding timelines and confirm your employer's HR team knows the sequence.
Frequently Asked Questions
Does a Senior Clinical Research Scientist role qualify as an H-1B specialty occupation?
Yes. USCIS treats Senior Clinical Research Scientist positions as specialty occupations because the role normally requires at least a bachelor's degree in a directly related field such as pharmacology, biochemistry, or clinical science. Senior-level roles often carry an expectation of an advanced degree, which further supports the specialty occupation determination.
Which visa types are realistic for this role if I'm not subject to the H-1B cap?
If you're already in H-1B status, you can transfer to a new employer once the new petition is filed, with no waiting period required. Australians can pursue the E-3 visa, which has a separate cap and no lottery. Chilean and Singaporean nationals may qualify for the H-1B1 visa. TN visa status does not cover clinical research scientist roles, as the position isn't on the USMCA profession list.
How do I find employers who actively sponsor visas for clinical research scientists?
Migrate Mate lists employers with verified LCA filing history for clinical and life sciences research roles, so you can focus your search on companies with a documented track record of sponsorship rather than relying on job description language alone.
Can I use OPT or STEM OPT while working as a Senior Clinical Research Scientist?
Yes, if your degree is in a qualifying STEM field such as biological sciences, pharmacology, or biostatistics, your role will typically satisfy the degree-to-job alignment requirement for STEM OPT. Your employer must be enrolled in E-Verify to sign your Form I-983 training plan. STEM OPT provides 24 months of additional work authorization beyond initial OPT, giving you more runway to secure H-1B sponsorship.
What does the green card process look like for a Senior Clinical Research Scientist?
Most employer-sponsored green cards for this role follow the EB-2 or EB-3 pathway, both of which require PERM labor certification filed with DOL before USCIS can adjudicate the immigrant petition. EB-2 requires an advanced degree or exceptional ability. Processing timelines vary significantly based on your country of birth, with Indian and Chinese nationals facing priority date backlogs. Self-petition under the EB-2 National Interest Waiver is also available if your research serves a national interest goal.
What is the prevailing wage requirement for sponsored Senior Clinical Research Scientist 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.