Clinical Research Associate III

CVRx | Barostim

. Execute day-to-day operations associated with clinical trials .

Posted 9/24/2026full-timeBrooklyn Park • Minnesota • United StatesJuniorMid-Level💰 $127,000 - $142,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in clinical trial operations, including compliance with GCP and regulatory guidelines, site monitoring, and data management. Proven ability to manage relationships with clinical sites and support project deliverables effectively.

Highest-signal resume keywords

Clinical Trial MonitoringGCP ComplianceRegulatory Documentation ManagementData Quality EvaluationClinical Research Experience

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial OperationsRegulatory ComplianceData AnalyticsMonitoring Reports PreparationRisk Mitigation PlanningDevice Accountability ManagementStudy Protocol DevelopmentEnrollment Trend AnalysisTrial Master File DocumentationIRB Submission Support

Soft Skills

Attention to DetailEffective CommunicationProblem-SolvingTeam CollaborationAdaptability

Certifications & Qualifications

Bachelor's Degree

Industry Keywords

Clinical ResearchImplantable Medical DeviceSOPsEthics CommitteeMedical TerminologyHigh-Growth EnvironmentCross-Functional CollaborationVendor OversightQuality Management SystemClinical Operations Optimization

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

Execute day-to-day operations associated with clinical trials
Monitor clinical trial sites for compliance with study protocols, SOPs, CVRx requirements, GCP, and applicable regulations
Work closely with the Clinical Study Manager to meet project deliverables
Develop and maintain working relationships with study sites as the primary point of contact
Assist with preparation of study materials and training of investigators and site staff
Support site IRB or ethics committee submissions
Collect and track required regulatory documents from Clinical Centers
Coordinate and conduct monitoring at participating centers
Prepare and submit monitoring reports
Evaluate site performance using enrollment trends, data quality metrics, protocol deviations, product accountability, and patient safety parameters
Support AE/SAE identification, documentation, and reporting
Verify safety documentation, device complaint forms, and follow-up queries
Identify site-level risks and support risk-mitigation plans
Source-verify clinical data and oversee data correction
Maintain Clinical Study files and Trial Master File documentation
Manage device accountability at sites, when applicable
Process payments to sites, vendors, and consultants
Review center activation documentation
Collaborate with Clinical Project Management, Data Management, Safety, Regulatory, Quality, and Training
Provide operational input on protocols, CRFs, risk assessments, monitoring plans, investigational brochures, and essential documents
Contribute to TMF quality checks, process improvements, QMS updates, and clinical operations optimization
Assist with metrics reporting, monitoring dashboards, and early risk detection through data analytics
Participate in vendor oversight
Train and mentor Clinical Research Associates and internal team members
Interface with Regulatory Affairs, Quality Assurance, Research & Development, U.S. Market Development, Commercial Development, and Clinical Research Organizations
Complete special projects and assigned job-related duties

Requirements

What you’ll need

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
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
May be required to be fully vaccinated against the COVID-19 virus and other diseases

Benefits

Comp & perks

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
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