Sign up to access all features of our service.
  • Job search
  • Favorites
  • Create a CV
    New
  • Salaries
  • Subscriptions

Clinical & Regulatory Affairs

Anteris Technologies

Job Description

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.

Vacancy posted 8 days ago
Similar jobs that could be interesting for youBased on the Clinical & Regulatory Affairs in Minneapolis, MN vacancy
  • $85k - $95k

     ...Regulatory And Clinical Specialist As a global medtech company, we are driven by our Vision of changing the trajectory of lives for a new...  ...experience in medical writing and medical device regulatory affairs or a Ph.D. with at least 3 years of experience Location... 
    Suggested
    Remote work
    Worldwide
    Flexible hours

    LivaNova

    Minneapolis, MN
    1 day ago
  • Optum in the United States is seeking a Senior M&R Coding Clinical Analyst to validate claims by comparing provider submissions with medical records. This remote role offers flexibility to telecommute from anywhere in the U.S. and requires careful judgment in line with... 
    Suggested
    Remote job

    Stryker Corporation

    Minneapolis, MN
    3 days ago
  • A medical consulting firm is seeking a Clinical Subject Matter Expert (SME) to support device risk management activities. The ideal candidate will have a degree in a clinical field (RN, MD) and at least 10 years of clinical experience, particularly within an FDA regulated... 
    Suggested

    Deegit Inc

    Minneapolis, MN
    2 days ago
  • Optum is seeking a M&R Coding Clinical Analyst to verify claim accuracy by comparing provider records to medical documentation, applying CPT/HCPCS/ICD coding rules and compliance policies. You will assess service levels and potential billing issues in a telecommuting environment... 
    Suggested
    Remote job

    Sacbar

    Minneapolis, MN
    3 days ago
  • $107.2k - $160.8k

     ...he Regulatory Affairs Specialist is responsible for day-to-day regulatory affairs tasks required to maintain compliance with Coloplast’s quality...  ...approve IFU, labels and promotion material Work with Clinical and Quality to prepare post-market data for inclusion in... 
    Suggested
    Full time
    Work at office
    Local area
    Immediate start
    Flexible hours

    Coloplast A/S

    Minneapolis, MN
    1 day ago
  • Job Description: Highly experienced Principal Regulatory Affairs Specialist to lead and support global post-market regulatory compliance activities...  ...training to internal teams. Collaborate with Quality, Clinical, Engineering, Manufacturing, and Commercial teams to ensure... 

    Katalyst Healthcares & Life Sciences

    Minneapolis, MN
    3 days ago
  • $62.3k - $102.35k

     ...Advanced Regulatory Affairs SpecialistBy joining Bio-Techne, you'll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further... 
    Contract work
    Temporary work
    Internship
    Worldwide
    Flexible hours

    Bio-Techne

    Minneapolis, MN
    2 days ago
  •  ...advancements in cardiac care through its innovative structural heart technologies. The company seeks professionals for Clinical & Regulatory Affairs roles to support clinical research and regulatory strategies critical for breakthrough therapies. Join a team that values... 

    Anteris Technologies

    Osseo, MN
    4 days ago
  •  ...equivalent) and experience with healthcare provider strategy and operations are highly preferred5+ years of experience in a hospital/clinical setting, specifically within workforce management, staffing office operations, or clinical labor consultingDeep interest or... 
    Apprenticeship
    Work at office
    Easy work

    McKinsey & Company

    Minneapolis, MN
    1 day ago
  • $189k - $246k

     ...Department: 107000 Regulatory Location: San Diego, USA- Remote Position Summary The Director, Regulatory Affairs Strategy is responsible for developing and executing global regulatory...  ...programs to support successful clinical development, registration, and commercialization... 
    Temporary work
    Local area
    Remote work
    Weekend work

    Travere Therapeutics

    Minneapolis, MN
    1 day ago
  • $85.1k - $161.7k

     ...why there’s nowhere like RSM.We are currently seeking an Epic Clinical Subject Matter Expert & Project Manager to join our Healthcare...  ...adoption. Ensure solutions align with Epic Systems best practices, regulatory expectations, and long-term sustainability. Support... 
    Full time
    Work experience placement
    Internship
    Local area
    Immediate start

    RSM International

    Minneapolis, MN
    11 hours ago
  •  ...Minneapolis, MNEmployment Type: C2CIndustry: Computer SoftwareClient: WiproContact: Meghana GorusuCompany: SRI Tech SolutionsJob Title: Clinical Informaticist Analyst - 12 PositionsLocation: Minneapolis, MN (Remote)Profiles with more emphasis on the following:The Clinical... 
    Remote work

    SRI Tech

    Minneapolis, MN
    2 days ago
  • $171k - $273k

     ...Director Of Regulatory Affairs - RespirTech The Director of Regulatory Affairs will lead the Philips RespirTech InCourage Vest Therapy...  ...partnerships with key stakeholders including R&D, Marketing, Quality, Clinical Affairs and other functions at all levels within the... 
    Work visa
    Relocation package

    Philips

    Minneapolis, MN
    2 days ago
  •  ...our employees experience every day.The Associate Director, Regulatory Affairs - Pulsed Field Ablation (PFA) is responsible for leading global...  ...compliance initiatives.You will partner closely with R&D, clinical, quality, medical safety, operations, program management, and... 
    Hourly pay
    Worldwide
    Shift work

    Boston Scientific Corporation

    Arden Hills, MN
    4 days ago
  • A medical device company is seeking a Clinical Research Associate to manage and monitor global clinical studies ensuring compliance with regulatory requirements. This remote position aims to support study site management and assists in the development of clinical study... 
    Remote work

    HistoSonics, Inc.

    Minneapolis, MN
    2 days ago
  • $94k - $128k

     ...Job description Job Summary The Senior Clinical Data Analyst independently executes assigned clinical studies activities, applying comprehensive...  ..., and operational workflows. · Ensures compliance with regulatory, data privacy, and ethical standards · Works independently on... 
    Work experience placement
    Local area
    Remote work

    GrabJobs

    Minneapolis, MN
    2 days ago
  •  ...medication in an accurate and timely manner in accordance with all legal, regulatory agency and Fairview requirements.Coordinate ordering, delivery of medications, supplies and equipment to multiple clinical areas as requested.Data collection, reporting, process improvement... 
    Temporary work
    Relocation package
    Flexible hours
    Rotating shift

    Ebenezer

    Minneapolis, MN
    4 days ago
  •  ...Health Records Analyst to design, support, and optimize EHR solutions within our behavioral health systems. You will collaborate with clinical revenue cycle teams and IT staff through all project phases, from requirements gathering to testing and post-implementation... 

    Socket.dev

    Minneapolis, MN
    1 day ago
  • UnitedHealth Group is seeking a M&R Coding Clinical Analyst to verify the accuracy of provider claims by comparing medical records to submitted data. This role requires independent judgment on complex payment decisions while ensuring compliance with state and federal guidelines... 
    Remote job

    Texas Health Institute

    Minneapolis, MN
    3 days ago
  • $171k - $273k

    Job TitleDirector of Regulatory Affairs - RespirTech (Plymouth, MN)Job DescriptionDirector of Regulatory Affairs - RespirTech (Plymouth, MN...  ...partnerships with key stakeholders including R&D, Marketing, Quality, Clinical Affairs and other functions at all levels within the... 
    Full time
    Work at office
    Immediate start
    Work visa
    Relocation package
    3 days per week

    Philips

    Plymouth, MN
    4 days ago
  •  ...Experienced Clinical Research Associate - Sponsor Dedicated Syneos Health is a leading...  .... We translate unique clinical, medical affairs and commercial insights into outcomes to...  ...performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good... 
    Contract work
    Interim role
    Local area
    Immediate start
    Remote work
    Flexible hours

    Syneos Health/ inVentiv Health Commercial LLC

    Minneapolis, MN
    2 days ago
  •  ...Medtronic Global Regulatory Affairs Team Member Careers that change lives start here. Medtronic is a global leader in healthcare technology...  ...for a highly motivated and skilled individual to join our Clinical Research, Medical Science, and Regulatory Affairs... 
    H1b
    Work at office
    Local area
    Immediate start
    Flexible hours
    Shift work

    Minnesota Jobs

    Minneapolis, MN
    4 days ago
  • $18.76 - $23.45 per hour

     ...strong sense of purpose in their roles, contributing to a familial atmosphere characterized by mutual respect and enjoyment. The Clinic Patient Registration Specialist provides initial access for all clinic and Orthopedic Urgent Care patients including responsibility... 
    Hourly pay
    Full time
    Work at office
    Local area
    Monday to Friday
    Flexible hours

    Summit Orthopedics

    Minneapolis, MN
    2 days ago
  • hmr is looking for a Clinic Supervisor in Plymouth, Minnesota, to oversee daily operations at the clinic, ensuring efficient workflows and exceptional patient experiences. This role includes supervising administrative staff and supporting training initiatives while maintaining... 

    hmr

    Minneapolis, MN
    4 days ago
  • Job-ID31513809Reference25-04468 Job Description: The Senior Regulatory Affairs Manager will play a crucial role in leading and managing the regulatory submissions, including 510(k) and submissions. This individual will ensure compliance with all applicable regulations... 

    Katalyst Healthcares & Life Sciences

    Minneapolis, MN
    2 days ago
  • $61.3k - $122.7k

     ...The Opportunity Abbott is seeking a passionate, experienced Regulatory Affairs Specialist II to join our team on-site in Plymouth, MN. This...  ...timelines to project teams. Evaluate proposed preclinical, clinical, design and manufacturing changes for regulatory submission... 
    Flexible hours

    Abbott

    Minneapolis, MN
    2 days ago
  •  ...understand requirements of pertinent federal, state and local regulatory schemes in reference to all business units within the organization...  ...a fast?moving environmentBackground in compliance, regulatory affairs, or similarExperience with large, complex organizations,... 
    Local area

    Omni Inclusive

    Minneapolis, MN
    3 days ago
  •  ...Regulatory Affairs SpecialistThis role is ideal for a regulatory professional with strong experience in FDA, Health Canada, and EU medical...  ...technical files, including risk assessments, usability reports, and clinical evaluationsPrepare and execute annual regulatory... 
    Work at office

    Oxenham Group

    Saint Paul, MN
    11 hours ago
  • Medtronic plc busca un Especialista en Asuntos Regulatorios para desarrollar estrategias de registro mundial y apoyar la presentación de expedientes ante agencias regulatorias como FDA y EU MDR. Se requiere experiencia en dispositivos médicos, conocimientos de normativas...

    Medtronic Plc

    Minneapolis, MN
    3 days ago
  • $113.03k - $165.77k

     ...job is to strategically plan, execute and provide oversight to regulatory activities necessary to obtain and maintain regulatory...  ...product submissions, identifying needs for bench, animal and clinical testing. 3. Provides strategic input. Participates on Product... 
    Full time
    Immediate start

    Integer Holdings Corporation

    Plymouth, MN
    1 day ago

Do you want to receive more vacancies?

Subscribe and receive similar vacancies to Clinical & Regulatory Affairs. Be the first to apply!