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Scientific Affairs Associate Jobs in Minnesota (NOW HIRING)

... Associate or Bachelor's degree, preferably in the science or engineering disciplines Must have 2-5 years in a medical device organization, preferably in regulatory affairs Previous US, Canadian, and ...

... Associate or Bachelor's degree, preferably in the science or engineering disciplines • Must have 2-5 years in a medical device organization, preferably in regulatory affairs • Previous US ...

Support research initiatives as requested by AbbVie R&D, Clinical Operations, and Medical Affairs ... Physician Associate or Nurse Practitioner) in a relevant scientific discipline. Doctorate strongly ...

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Scientific Affairs Associate information

What does a Scientific Affairs Associate do?

A Scientific Affairs Associate supports the development and communication of scientific information within organizations such as pharmaceutical, biotechnology, or medical device companies. Their responsibilities often include reviewing and summarizing scientific literature, preparing technical documentation, assisting with regulatory submissions, and serving as a liaison between research, regulatory, and commercial teams. They play a crucial role in ensuring scientific accuracy in company materials and helping translate complex data into understandable information for both internal and external stakeholders. This position typically requires a strong background in science, excellent communication skills, and attention to detail.

What are the key skills and qualifications needed to thrive as a Scientific Affairs Associate?

To thrive as a Scientific Affairs Associate, a strong background in life sciences, analytical thinking, and often an advanced degree (such as MS or PhD) are essential. Familiarity with regulatory databases, scientific literature search tools, and document management systems is typically required, along with experience in preparing scientific and regulatory documents. Excellent communication, attention to detail, and the ability to collaborate with cross-functional teams are standout soft skills for this role. These competencies are crucial for ensuring accurate scientific communication, regulatory compliance, and effective support of product development and approval processes.

How does a Scientific Affairs Associate typically collaborate with cross-functional teams in a healthcare or pharmaceutical company?

As a Scientific Affairs Associate, you will frequently work alongside clinical, regulatory, and marketing teams to ensure scientific accuracy and compliance in all communications and materials. Collaboration often involves reviewing clinical data, preparing scientific content for internal and external stakeholders, and supporting product launches or educational initiatives. This role requires clear communication and the ability to translate complex scientific information for diverse audiences, making teamwork and adaptability essential for success.

What cities in Minnesota are hiring for Scientific Affairs Associate jobs?

Cities in Minnesota with the most Scientific Affairs Associate job openings:

Infographic showing various Scientific Affairs Associate job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 71% Full Time, 22% Part Time, 1% Temporary, and 5% Contract. Highlights an 96% Physical, 1% Hybrid, and 3% Remote job distribution.

Clinical & Regulatory Affairs

Minneapolis, MN • On-site

Anteris Technologies
Medical Equipment and Supplies Manufacturing • 51 - 200 employees

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 26 days ago


Job description

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.

Anteris Technologies is advancing innovative structural heart technologies designed to redefine expectations in the treatment of aortic stenosis. Our Clinical and Regulatory Affairs teams play a critical role in supporting clinical research, physician engagement, global regulatory strategy, and the advancement of breakthrough therapies through development and commercialization.

We are interested in connecting with professionals with the following experience:

  • Clinical operations
  • Clinical monitoring
  • Physician support
  • Field clinical education
  • Global regulatory compliance, or
  • Clinical trial management within the medical device industry.

Roles in Clinical & Regulatory Affairs include:

  • Clinical Project Manager
  • Clinical Research Associate
  • Clinical Research Scientist
  • Clinical Specialist
  • Regulatory Affairs Specialist

Candidates with experience supporting Class III medical devices, structural heart therapies, cardiovascular technologies, or global clinical studies are especially encouraged to apply. Successful candidates are collaborative, adaptable, organized, and comfortable operating within fast-paced, cross-functional environments.

This is an opportunity to contribute directly to meaningful innovation while helping bring transformative therapies to patients worldwide.

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 Equity Program
  • Paid Holidays & Vacation
  • Employee Assistance Program
  • Inclusive Team Environment

These evergreen postings are designed to connect us with talented individuals interested in future opportunities at Anteris Technologies. Because openings may vary over time, additional details regarding specific responsibilities, qualifications, work arrangements, and compensation will be shared as candidates move forward in the process for individual roles.

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.