Remote Clinical Research Associate III - Impactful Trials

CVRx, Inc.; Brooklyn Park (MN); Hybrid; USD 127,000 - 142,000; Full time

Benefits offered by this job

Health & Dental Insurance

HSA contributions

401(k) match

ESPP & RSU grants

Company stock options

Holidays & generous PTO

Parental leave

Job summary

CVRx, Inc. is seeking a Clinical Research Associate III (CRAIII) to manage day-to-day operations of clinical trials and monitor sites to ensure compliance with the protocol, SOPs, and GCP.

The role collaborates with the Clinical Study Manager to meet project deliverables and can work from the CVRx office or at sites during monitoring. Ideal candidates will reside near our Brooklyn Park, MN headquarters with willingness for occasional on-site visits and up to 50% travel within the US to support

Qualifications

• Bachelor's degree required.
• Minimum of 5 years' experience directly supporting clinical research of an implantable medical device or similar medical/scientific area.
• Minimum of 2 years' experience in monitoring clinical trial sites.
• Deep knowledge of GCPs and regulatory guidelines for clinical trials.
• Excellent written and oral communication skills and ability to work cross-functionally.

Responsibilities

• Develops and maintains relationships with study sites; primary contact.
• Supports material preparation and investigator/site staff training.
• Monitors sites per plan to ensure protocol and regulatory compliance.
• Collects and tracks regulatory documents from sites.
• Verifies data accuracy and oversees data correction with site personnel.
• Prepares monitoring reports per study requirements.
• Contributes to TMF quality checks and trial documentation.

Skills

Clinical research

Site monitoring

GCP knowledge

Regulatory compliance

Medical terminology

Education

Bachelor's degree

Advanced degree preferred

Job description

CVRx, Inc. is seeking a Clinical Research Associate III (CRAIII) to manage day-to-day operations of clinical trials and monitor sites to ensure compliance with the protocol, SOPs, and GCP.

The role collaborates with the Clinical Study Manager to meet project deliverables and can work from the CVRx office or at sites during monitoring. Ideal candidates will reside near our Brooklyn Park, MN headquarters with willingness for occasional on-site visits and up to 50% travel within the US to support