Clinical Research Associate (CRA) III
CVRx · 5a90b016-c0c5-4a41-9aed-020de830b96e
Normalized fields
open- Function
- digital_it
- Business unit
- Not classified
- Location
- Brooklyn Park, MN; USA
- Work model
- Hybrid
- Seniority
- Not classified
- Clearance
- Not provided
- Employment type
- Full-Time
- Compensation
- {"text":"pay high level of attention to details and accuracy","period":null,"maximum":null,"minimum":null,"currency":null}
- First seen
- 2026-09-25T13:00:24.719Z
- Last seen
- 2026-10-12T13:00:46.477Z
- Requisition
- 5a90b016-c0c5-4a41-9aed-020de830b96e
Latest version
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 mostly remote with travel to various sites across the southern US. Please note that if our ideal candidates reside near our headquarters in Brooklyn Park, MN we ask that you be open to occasional on-site visits to our HQ for meetings, as required. Travel: Please note that this position requires travel up to 50% as needed to support monitoring in sites across the US. The Role The Clinical Research Associate III (CRA III) will be responsible for the day-to-day operations associated with the execution of clinical trials and monitoring the clinical trial sites to ensure they are complying to the applicable study protocol, Standard Operating Procedures (SOPs), CVRx requirements, Good Clinical Practice (GCP), and the applicable regulatory requirement(s). The CRA III will work closely with the Clinical Study Manager to ensure site day-to-day operations and monitoring 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 and serves as the primary point of contact. Assists in preparation of study materials and training of investigators and site staff. Supports Clinical Centers in the execution of site IRB or ethics committee submissions. Collects and tracks required regulatory documents from various Clinical Centers as assigned. 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 Evaluates site performance through analysis of enrollment trends, data quality metrics, protocol deviations, product accountability, and patient safety parameters. Supports sites in AE/SAE identification, documentation, and reporting. Verifies timely submission of required safety documentation, device complaint forms, and follow-up queries. Drives proactive risk identification at the site level and support the execution of risk-mitigation plans. Sources and verifies clinical data/information and oversees data correction to 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. Works closely with Clinical Project Managers, Data Management, Safety, Regulatory, Quality, and Training to ensure end-to-end study execution. Provides operational input on protocol development, CRFs, risk assessments (RACT), monitoring plans, investigational brochures, and essential document requirements. Collaborates in Trial Master File (TMF) on quality checks to ensure site-level documentation is complete, audit-ready, and compliant. Contributes to process improvement initiatives, QMS updates, and clinical operations optimization. Assist management in metrics reporting, monitoring dashboards, and early risk detection through data analytics. Participates 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 Affairs and Quality Assurance, Research & Development, U.S. Market Development, Commercial Development and Clinical Research Organizations. Provides mentoring regarding site monitoring to internal team. Completes special projects and performs other job-related duties as assigned. REQUIRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE Bachelor’s degree Minimum of 5 years’ experience directly supporting clinical research of an implantable medical device or similar experience in a medical/scientific area Minimum of 2 years’ experience in monitoring clinical trial sites Deep knowledge of GCP’s and regulatory compliance guidelines for clinical trials Effective comprehension of medical terminology Ability to pay high level of attention to details and accuracy Excellent at managing multiple tasks and able to operate independently Manage tasks and duties in an efficient and expedient manner Maintains a high personal standard for ethics and integrity Contributing team player with excellence in working cross-functionally while maintaining high-performance standards Comfortable in a small company and able to thrive in a high-growth environment Sophisticated written and oral communications skills Effective problem-solving skills Adaptable, resourceful, and comfortable navigating change Entrepreneurial approach Must be able to travel up to 40% within the US by car and air Must possess valid government ID for domestic air travel (i.e. Passport, etc.) Must have valid license and reliable transportation Must have a professional home-office environment in which to perform work from home (when permitted) in a confidential and private manner 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 high speed internet connection required when working in a home office Must be able to sit/stand/walk 8 hours per day Position requires up to 40% travel across the U.S. 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. 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 hiring@cvrx.com CVRx Privacy Policy CVRx SMS Terms of Service This requisition will be open until filled.
Derived classifications
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2 retained{
"added": [
"This position is mostly remote with travel to various sites across the southern US.",
"Please note that if our ideal candidates reside near our headquarters in Brooklyn Park, MN we ask that you be open to occasional on-site visits to our HQ for meetings, as required.",
"Travel: Please note that this position requires travel up to 50% as needed to support monitoring in sites across the US.",
"Assists in preparation of study materials and training of investigators and site staff.",
"Supports Clinical Centers in the execution of site IRB or ethics committee submissions.",
"Collects and tracks required regulatory documents from various Clinical Centers as assigned.",
"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 Evaluates site performance through analysis of enrollment trends, data quality metrics, protocol deviations, product accountability, and patient safety parameters.",
"Supports sites in AE/SAE identification, documentation, and reporting.",
"Verifies timely submission of required safety documentation, device complaint forms, and follow-up queries.",
"Drives proactive risk identification at the site level and support the execution of risk-mitigation plans.",
"Sources and verifies clinical data/information and oversees data correction to 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.",
"Works closely with Clinical Project Managers, Data Management, Safety, Regulatory, Quality, and Training to ensure end-to-end study execution.",
"Provides operational input on protocol development, CRFs, risk assessments (RACT), monitoring plans, investigational brochures, and essential document requirements.",
"Collaborates in Trial Master File (TMF) on quality checks to ensure site-level documentation is complete, audit-ready, and compliant.",
"Contributes to process improvement initiatives, QMS updates, and clinical operations optimization.",
"Assist management in metrics reporting, monitoring dashboards, and early risk detection through data analytics.",
"Participates 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.",
"Market Development, Commercial Development and Clinical Research Organizations.",
"Provides mentoring regarding site monitoring to internal team.",
"Completes special projects and performs other job-related duties as assigned.",
"REQUIRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE Bachelor’s degree Minimum of 5 years’ experience directly supporting clinical research of an implantable medical device or similar experience in a medical/scientific area Minimum of 2 years’ experience in monitoring clinical trial sites Deep knowledge of GCP’s and regulatory compliance guidelines for clinical trials Effective comprehension of medical terminology Ability to pay high level of attention to details and accuracy Excellent at managing multiple tasks and able to operate independently Manage tasks and duties in an efficient and expedient manner Maintains a high personal standard for ethics and integrity Contributing team player with excellence in working cross-functionally while maintaining high-performance standards Comfortable in a small company and able to thrive in a high-growth environment Sophisticated written and oral communications skills Effective problem-solving skills Adaptable, resourceful, and comfortable navigating change Entrepreneurial approach Must be able to travel up to 40% within the US by car and air Must possess valid government ID for domestic air travel (i.e.",
"Candidates must be legally authorized to work in the United States without current or future sponsorship.",
"CVRx is proud to offer competitive salaries and benefits plans."
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"removed": [
"This position is mostly remote.",
"Please note that our ideal candidates will reside near our headquarters in Brooklyn Park, MN and be open to occasional on-site visits for meetings as required.",
"Please note that this position requires travel up to 50% as needed to support monitoring in sites across the US.",
"Assists in preparation of study materials and training of investigators and site staff 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 verifies clinical data/information and oversees data correction to 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.",
"Market Development, Commercial Development and Clinical Research Organizations Provides mentoring regarding site monitoring to internal team Completes special projects and performs job-related duties as assigned REQUIRED EDUCATION, TRAINING AND JOB-RELATED EXPERIENCE Bachelor’s degree Minimum of 5 years’ experience directly supporting clinical research of an implantable medical device or similar experience in a medical/scientific area Minimum of 2 years’ experience in monitoring clinical trial sites Deep knowledge of GCP’s and regulatory compliance guidelines for clinical trials Effective comprehension of medical terminology Ability to pay high level of attention to details and accuracy Excellent at managing multiple tasks and able to operate independently Manage tasks and duties in an efficient and expedient manner Maintains a high personal standard for ethics and integrity Contributing team player with excellence in working cross-functionally while maintaining high-performance standards Comfortable in a small company and able to thrive in a high-growth environment Sophisticated written and oral communications skills Effective problem-solving skills Adaptable, resourceful, and comfortable navigating change Entrepreneurial approach Must be able to travel up to 40% within the US by car and air Must possess valid government ID for domestic air travel (i.e.",
"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."
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