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Medical Device Clinical Jobs in Minnesota (NOW HIRING)

Abbott

Senior Clinical Scientist

New Brighton, MN

$100K - $200K/yr

  • Medical

  • Retirement

Experience conducting medical device clinical trials preferred (TAVR in particular). Investigational Device Exemption (IDE) trial experience. Physician management. Safety management desirable.

Abbott

Senior Clinical Scientist

New Brighton, MN · On-site

$100K - $200K/yr

  • Medical

  • Retirement

Experience conducting medical device clinical trials preferred (TAVR in particular). Investigational Device Exemption (IDE) trial experience. Physician management. Safety management desirable.

Socket.dev

Study Director

Minneapolis, MN · On-site

$90 - $125/hr

  • Medical

  • Dental

  • Vision

  • Retirement

Bright Research is a dynamic and growing medical device Clinical Research Organization (CRO) located in downtown Minneapolis. We manage clinical trials from concept to completion, with smarts and ...

Exelare

Clinical Specialist

Minneapolis, MN · On-site

Clinical Specialist Medical device manufacturer is looking to fill a "clinical specialist" position. This is not a sales position. You will be working with the most exciting, high tech operating room ...

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Showing results 21-40

All JobsMedical Device Clinical JobsMedical Device Clinical Jobs in Minnesota

Medical Device Clinical information

See Minnesota salary details

$97.5K

$110.2K

$121.4K

How much do medical device clinical jobs pay per year?

As of Aug 19, 2026, the average yearly pay for medical device clinical in Minnesota is $110,183.00, according to ZipRecruiter salary data. Most workers in this role earn between $103,800.00 and $116,600.00 per year, depending on experience, location, and employer.

What is a medical device clinical professional?

Medical Device Clinical professionals are specialists who oversee and manage the clinical aspects of medical device development and testing. They are responsible for planning, executing, and monitoring clinical trials to ensure medical devices are safe and effective for patient use. Their work involves collaborating with regulatory bodies, healthcare providers, and research organizations to collect and analyze clinical data. These professionals play a key role in ensuring that medical devices comply with regulatory requirements before they reach the market.

What are the key skills and qualifications needed to thrive as a medical device clinical specialist?

To thrive as a Medical Device Clinical Specialist, you need a solid background in life sciences or nursing, strong clinical knowledge, and often a relevant degree or certification. Familiarity with medical device technologies, regulatory standards, and clinical trial management systems is typically required. Excellent communication, problem-solving, and relationship-building skills help you effectively train healthcare professionals and support product adoption. These skills are crucial for ensuring safe, effective device use and successful integration into clinical environments.

What are some common challenges faced by professionals in medical device clinical roles, and how can they be addressed?

Professionals in Medical Device Clinical roles often encounter challenges such as navigating complex regulatory requirements, coordinating multi-site clinical trials, and ensuring timely patient recruitment. To address these, strong organizational skills, clear communication with cross-functional teams, and ongoing education about evolving regulations are essential. Building strong relationships with investigators and site staff can also help streamline trial processes and ensure high-quality data collection.

What is the difference between Medical Device Clinical vs Medical Device Quality Assurance?

AspectMedical Device ClinicalMedical Device Quality Assurance
CertificationsClinical Research Certification, GCP trainingISO 13485, GMP training
Work EnvironmentHospitals, clinics, clinical research settingsManufacturing facilities, quality labs
Employer & Industry UsageMedical device companies, research organizationsManufacturers, regulatory agencies
Primary FocusClinical trials, patient safety, device efficacyProduct quality, compliance, process validation

Medical Device Clinical roles focus on conducting clinical trials and ensuring device safety and efficacy, often working directly with patients. In contrast, Medical Device Quality Assurance emphasizes maintaining product quality, regulatory compliance, and manufacturing standards. Both roles are essential in the medical device industry but serve different functions within the product lifecycle.

What does a medical device clinical specialist do?

A medical device clinical specialist is responsible for training healthcare professionals on the proper use of medical devices, providing technical support, and ensuring compliance with regulatory standards. They often work closely with sales teams, conduct product demonstrations, and gather user feedback to improve device performance and safety.

What cities in Minnesota are hiring for Medical Device Clinical jobs?

Cities in Minnesota with the most Medical Device Clinical job openings:

Medical Device Clinical jobs near you
Infographic showing various Medical Device Clinical job openings in Minnesota as of August 2026, with employment types broken down into 1% As Needed, 76% Full Time, 15% Part Time, 7% Contract, and 1% Nights. Highlights an 89% Physical, 1% Hybrid, and 10% Remote job distribution, with an average salary of $110,183 per year, or $53 per hour.

Senior Clinical Scientist

Abbott

New Brighton, MN

$100K - $200K/yr

Full-time

Medical, Retirement

Posted 19 days ago

Abbott rating

7.8

Company rating: 7.8 out of 10

Based on 138 frontline employees who took The Breakroom Quiz

176th of 540 rated manufacturers

Job description

Abbott is a global healthcare leader that helps people live more fully at all stages of life. Our portfolio of life-changing technologies spans the spectrum of healthcare, with leading businesses and products in diagnostics, medical devices, nutritionals and branded generic medicines. Our 115,000 colleagues serve people in more than 160 countries.JOB DESCRIPTION:

At Abbott, you can do work that matters, grow, and learn, care for yourself and your family, be your true self, and live a full life. You'll also have access to:

Career development with an international company where you can grow the career you dream of.

Employees can qualify for free medical coverage in our Health Investment Plan (HIP) PPO medical plan in the next calendar year.

An excellent retirement savings plan with a high employer contribution

Tuition reimbursement, the Freedom 2 Save student debt program, and FreeU education benefit - an affordable and convenient path to getting a bachelor's degree.

A company recognized as a great place to work in dozens of countries worldwide and named one of the most admired companies in the world by Fortune.

A company that is recognized as one of the best big companies to work for as well as the best place to work for diversity, working mothers, female executives, and scientists.

The Opportunity

This position is part of our Structural Heart Division. Our business purpose is to restore health and improve quality of life by designing and providing device and management solutions for treating structural heart disease.

As the Senior Clinical Scientist, you'll have the chance to be responsible for the design, execution, and monitoring of internal and external clinical studies.

What You'll Work On

Develops and/or reviews departmental operating procedures.

Develops study protocols for executing experiments, evaluation, and documentation of results.

Follows standard and complex procedures in executing studies, evaluation, and documentation of results.

Participates in the development of clinical strategy for the product development.

Responsible for the design, execution and monitoring of Abbott sponsored external clinical studies including PMA and outcome studies.

Responsible for identification and qualification of external clinical sites.

Responsible for the development and maintaining of operating procedures.

Participates in the development of clinical strategy to support product development and market introduction.

Participates in cross functional team activities for product development including risk management.

Successful and timely completion of clinical studies directly impacts the ability to meet product development goals and product introduction timelines.

Required Qualifications

Bachelors Degree ( 16 years) In a related field and/or an equivalent combination of education and work experience.

Minimum 8 years in conducting clinical studies or related laboratory skills. Preferred Qualifications

Experience in medical device related studies is desirable.

Knowledge of regulations governing medical devices is desirable.

Experience conducting medical device clinical trials preferred (TAVR in particular). Investigational Device Exemption (IDE) trial experience. Physician management. Safety management desirable. Experience working with external clinical research committees (i.e. screening committees, DSMB, CEC).

Learn more about our health and wellness benefits, which provide the security to help you and your family live full lives: www.abbottbenefits.com Follow your career aspirations to Abbott for diverse opportunities with a company that can help you build your future and live your best life. Abbott is an Equal Opportunity Employer, committed to employee diversity

The base pay for this position is

$100,000.00 - $200,000.00

In specific locations, the pay range may vary from the range posted.

JOB FAMILY:Clinical Affairs / StatisticsDIVISION:SH Structural HeartLOCATION:United States > Santa Clara : 4551 Great America ParkwayADDITIONAL LOCATIONS:United States > Minnesota > St. Paul : 1225 Old Highway 8 NWWORK SHIFT:StandardTRAVEL:Yes, 10 % of the TimeMEDICAL SURVEILLANCE:NoSIGNIFICANT WORK ACTIVITIES:Continuous sitting for prolonged periods (more than 2 consecutive hours in an 8 hour day), Keyboard use (greater or equal to 50% of the workday)Abbott is an Equal Opportunity Employer of Minorities/Women/Individuals with Disabilities/Protected Veterans.EEO is the Law link - English: http://webstorage.abbott.com/common/External/EEO_English.pdfEEO is the Law link - Espanol: http://webstorage.abbott.com/common/External/EEO_Spanish.pdf

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