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Remote Imaging Research Jobs in Minnesota (NOW HIRING)

... imaging, injections and infusions, and specialty surgical procedures in the clinic and hospital ... Monitor, research, and correct claim denials within health plan requirements and document any ...

Remote Overnight Radiologist

Rochester, MN · On-site +1

$312K - $390K/yr

Experience and proficiency with typical ED/Inpatient Stat CT and MR neurological imaging is ... research goals of the department, additional onsite weekday daytime coverage is included. This ...

... advanced research. At NextSilicon, everything we do is guided by three core values ... Remote considered for exceptional candidates. As part of a software-defined hardware company, you ...

Provide field support to Lease Operations, R&D, and OEM Customers around the world. Serve to focus ... imaging, virtual machine creation, software licensing, database management, and computer repair.

Remote Imaging Research information

What is remote imaging research?

Remote imaging research involves studying and developing methods and technologies to capture, process, and analyze images from a distance, often using satellites, drones, or other remote sensors. This field is crucial for applications such as environmental monitoring, agriculture, urban planning, and disaster management. Researchers in this area work on improving imaging systems, data analysis techniques, and the interpretation of remotely sensed imagery to support scientific and practical objectives.

What are the key skills and qualifications needed to thrive as a remote imaging researcher?

To thrive as a Remote Imaging Researcher, you need a solid background in imaging science, data analysis, and research methodologies, often supported by a degree in fields like biomedical engineering, physics, or computer science. Familiarity with imaging software (such as MATLAB, ImageJ, or Python-based tools), statistical analysis programs, and possibly certifications in advanced imaging techniques are typically required. Attention to detail, problem-solving abilities, and strong communication skills help researchers collaborate effectively and interpret complex imaging data. These skills are critical for producing accurate research findings and advancing innovations in imaging technology from a remote setting.

What are some common challenges faced when working remotely in imaging research, and how can they be addressed?

One common challenge in remote imaging research is maintaining effective collaboration with colleagues, especially when working on complex data analyses or sharing large imaging datasets. To address this, teams often use secure cloud-based platforms and regular video meetings to ensure seamless communication and data sharing. Another challenge is ensuring access to specialized software and computational resources, which can usually be mitigated through remote desktop solutions or institutional VPNs. Staying organized and proactively communicating are key to overcoming the unique obstacles of remote work in this field.

What is the difference between Remote Imaging Research vs Remote Imaging Technician?

AspectRemote Imaging ResearchRemote Imaging Technician
CredentialsTypically requires a degree in imaging, computer science, or related fieldsOften requires technical certifications or training in imaging equipment
Work EnvironmentResearch labs, universities, or remote research settingsField sites, hospitals, or remote technical support environments
Industry UsageUsed mainly in academic, healthcare research, and technology developmentUsed in healthcare, imaging service providers, and technical support roles
Job FocusDeveloping and analyzing imaging techniques and dataMaintaining, troubleshooting, and operating imaging equipment

Remote Imaging Research and Remote Imaging Technician roles share overlapping skills in imaging technology but differ mainly in focus. Research roles emphasize development and analysis, often requiring advanced degrees, while technician roles focus on operational support and maintenance. Understanding these differences helps job seekers target the right positions based on their skills and career goals.

What are the most commonly searched types of Imaging Research jobs in Minnesota?

The most popular types of Imaging Research jobs in Minnesota are:

What are popular job titles related to Remote Imaging Research jobs in Minnesota?

For Remote Imaging Research jobs in Minnesota, the most frequently searched job titles are:

What cities in Minnesota are hiring for Remote Imaging Research jobs?

Cities in Minnesota with the most Remote Imaging Research job openings:

Infographic showing various Remote Imaging Research job openings in Minnesota as of August 2026, with employment types broken down into 79% Full Time, 7% Part Time, 2% Temporary, and 12% Contract. Highlights an 100% Remote job distribution.

Clinical Research Associate (CRA) III

CVRx, Inc.

Brooklyn Park, MN • On-site, Remote

Full-time

Medical, Dental, Life, Retirement, PTO

This job post has expired 3 days ago. Applications are no longer accepted.


Job description

Why work for CVRx?

CVRx pioneers' unique therapies that harness and harmonize the body's natural systems, benefiting society and making CVRx a universal role model in healthcare. We value our commitments to others and continue to overcome challenges through determination, collaboration and purpose. If our culture and values speak to you, and if you have a passion for cutting-edge medical technologies, join our team and our mission to help others live better lives.

This position is remote. Our ideal candidate will reside near our headquarters in Brooklyn Park, MN for occasional on-site visits.  

The Role
TheClinical Research AssociateIII(CRAIII) will be responsible for the day-to-day operations associated with the execution of clinical trials andmonitoringthe clinical trial sitesto ensure they arecomplying to the applicable study protocol, Standard Operating Procedures (SOPs),CVRxrequirements, GoodClinicalPractice (GCP), and the applicable regulatory requirement(s).The CRAIIIwill work closely withtheClinical Study Manager to ensure siteday-to-day operations andmonitoring is executed to meet project deliverables. CRA III is expected to work from the CVRx office, or at the sites when monitoring.  
KEY DUTIES AND RESPONSIBILITIES
  • Develops and maintains successful working relationships with study sites andserves asthe primary point of contact. 

  • Assists in preparation of study materials and training of investigatorsand sitestaff 

  • Supports Clinical Centers in the execution of site IRB or ethics committee submissions 

  • Responsible for the collection and tracking of required regulatory documents from Clinical Centers 

  • Coordinates and conducts monitoring (as directed by the monitoring plan) at participating centers to ensure compliance with the protocol and applicable regulations, as well as the timely receipt of accurate data and other required study documents 

  • Prepares and submits high-quality monitoring reports per study-specific requirements 

  • Evaluate site performance through analysis of enrollment trends, data quality metrics, protocol deviations, product accountability, and patient safety parameters 

  • Support sites in AE/SAE identification, documentation, and reporting 

  • Verify timely submission of required safety documentation, device complaint forms, and follow-up queries 

  • Drive proactive risk identification at the site level and support the execution of risk-mitigation plans 

  • Source verifiesclinical data/information and oversees data correctionto match source 

  • Maintains Clinical Study files 

  • Manages device accountability at site(if applicable) 

  • Processes payments to sites, vendors, and consultants 

  • Reviews clinical data/information and oversees data correction 

  • Reviews center activation documentation 

  • Work closely with Clinical Project Managers, Data Management, Safety, Regulatory, Quality, and Training to ensure end-to-end study execution 

  • Provide operational input on protocol development, CRFs, risk assessments (RACT), monitoring plans, investigational brochures, and essential document requirements 

  • Collaborate in Trial Master File (TMF) quality checks to ensure site-level documentation is complete, audit-ready, and compliant 

  • Contribute to process improvement initiatives, QMS updates, and clinical operations optimization 

  • Assist management in metrics reporting, monitoring dashboards, and early risk detection through data analytics 

  • Participate in vendor oversight (central labs, imaging, core labs) to ensure site compliance (if applicable) 

  • Assists in training new Clinical Research Associates 

  • Assists with successful conduct of assigned studies. This includes interfacing with representatives from key functional groups including Regulatory Affairsand Quality Assurance,Research & Development, U.S. Market Development, Commercial Developmentand Clinical Research Organizations 

  • Provides mentoring regardingsitemonitoringto internal team 

  • Completes special projects and performs job-related duties as assigned 

REQUIRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE
  • Bachelor's degree 

  • 5+ years experience directly supporting clinical research or similar experience in a medical/scientific area 

  • 2+ years experience in monitoring clinical trial sites 

  • Knowledge of GCP's and regulatory compliance guidelines for clinical trials 

  • Knowledge of medical terminology 

  • High attention to detail and accuracy 

  • Able to manage multiple tasks and operate independently 

  • Operates in an efficient and expedient manner 

  • High ethical standards and integrity 

  • Strong team player with experience working cross-functionally and maintaining high-performance standards

  • Comfortable in a small company and thrives in a high-growth environment 

  • Advanced written and oral communications skills 

  • Good problem-solving skills 

  • Adaptable, resourceful, and comfortable navigating change 

  • Entrepreneurial approach 

PREFERRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE
  • Advanced degree in a related field is preferred

WORKING CONDITIONS AND REQUIRED PHYSICAL EFFORT
  • Normal office conditions and a reliable internet connection when working in a home office
  • Must be able to sit/stand/walk 8 hours per day
  • Position requires up to 40% travel
  • May be required to be fully vaccinated against the COVID-19 virus and other diseases

CVRx is unable to provide employment visa sponsorship for this position. Candidates must be legally authorized to work in the United States without current or future sponsorship

What we offer:

CVRx is proud to offer competitive salaries and benefits plans.

We offer a culture of teamwork, collaboration, and positivity, where challenging the status quo is welcomed, continuous learning is valued, and each of us has an opportunity to make a significant impact in an exciting, purpose-driven startup environment while also having fun.

Salary range for U.S locations (USD): 127,000 - 142,000 per year.

The pay range is applicable across the U.S., complies with federal and local regulations and may vary based on factors such as experience, certification/education, market conditions, and specific location. 

We also offer a competitive and rewarding benefits package, details listed below:

  • Competitive Health & Dental Insurance options with generous Company contributions 
  • Company contributions to an HSA with a high deductible insurance plan selection
  • 401(k) with a company match
  • Employee stock purchase plan (ESPP) & stock option and RSU grants
  • 12 company-paid holidays per year in addition to a generous Flex PTO plan
  • Generous paid time off for new parents
  • Company-paid life insurance & disability options
  • Unlimited growth opportunities in a growing company
  • Endless training & learning opportunities
  • Flexible Schedule

EEO STATEMENT

CVRx, Inc. provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.   

This policy applies to all terms and conditions of employment, including recruiting, hiring, placement, promotion, termination, layoff, recall, transfer, leaves of absence, compensation, and training.  

If you're an independent, self-motivated individual with excellent interpersonal skills, a desire to do great things and have a background in medical devices, healthcare or a related field, we want to hear from you!   

If you need assistance or an accommodation due to a disability, you may contact us at [email protected] 

CVRx Privacy Policy 
CVRx SMS Terms of Service 

This requisition will be open until filled.

We may use artificial intelligence (AI) tools to support parts of the hiring process, such as reviewing applications, analyzing resumes, or assessing responses and identifying potential inconsistencies or verification signals in application materials based on available information. These tools assist our recruitment team but do not replace human judgment. Final hiring decisions are ultimately made by humans. If you would like more information about how your data is processed, please contact us.
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