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CVRx | Barostim

Clinical Research Associate II – Hybrid

CVRx | Barostim

Clinical Research Associate managing clinical trial operations in Brooklyn Park for CVRx's medical technologies. Ensuring site compliance and data quality from start to finish in clinical studies.

Posted 7/1/2026full-timeBrooklyn Park • Minnesota • 🇺🇸 United StatesJuniorMid-Level💰 $85,000 - $105,000 per yearWebsite

Tech Stack

Tools & technologies
Google Cloud Platform

About the role

Key responsibilities & impact
  • Proactively maintains timelines for assigned or requested deliverables
  • Develops and maintains successful working relationships with study sites and CVRx field staff
  • Assists in preparation of study materials and training of investigators and research site staff
  • Becomes proficient with all study databases, systems and company quality management system
  • Reviews and verifies clinical data/information and oversees data correction to match source
  • Acts a site manager and monitor to assigned sites as applicable per study requirements
  • Processes payments to sites, vendors, and consultants. Supports the Clinical Project Manager with study finance activities and tracking
  • Supports Clinical Centers in the execution of site Institutional Review Board (IRB) or ethics committee (EC) submissions
  • Responsible for the collection, tracking, and maintaining required study and regulatory documents from clinical centers through all phases of assigned projects
  • Prepares study materials and trains investigators and site staff
  • Responsible for shipment of study-related materials as applicable
  • Coordinates and conducts monitoring (as directed by the monitoring plan) at participating centers to ensure compliance with protocol, regulations, and the timely receipt of accurate data / other required study documents
  • Reviews and verifies clinical data/information and oversees data correction to match source
  • Reviews monitoring reports
  • Manages device accountability at site (if applicable)
  • Provides input to study budgets and project plan
  • Contributes to maintaining oversight of activities conducted by Contract Research Organizations (CRO’s) or other contractors on behalf of CVRx (if applicable)
  • Assists in training or mentorship of new Clinical Research Associates
  • Completes special projects and performs job-related duties as assigned

Requirements

What you’ll need
  • Bachelor’s degree or advanced degree in science or a related field, or equivalent work experience
  • 2-4 years experience directly supporting clinical research or similar experience in a medical/scientific area
  • Knowledge of medical terminology
  • Experience with GCP’s and regulatory compliance guidelines for clinical trials
  • High attention to detail and accuracy
  • Ability to manage multiple tasks and operate independently
  • Operates in an efficient and expedient manner
  • High ethical standards and integrity
  • Experience working on cross-functional teams
  • Comfortable in a small company and thrives in a high-growth environment
  • Advanced written and oral communications skills
  • Good problem-solving skills
  • Adaptable and embraces change
  • Creative and resourceful
  • Team player with high performance standards
  • Entrepreneurial approach

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 restricted stock unit 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

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools
Clinical ResearchData ManagementRegulatory ComplianceGCP KnowledgeStudy BudgetingMonitoring ProtocolsClinical Data ReviewStudy DocumentationEthics Committee SubmissionsDevice Accountability
Soft Skills
Attention to DetailProblem-SolvingAdaptabilityTeam CollaborationEffective Communication