Join CVRx as a Clinical Research Associate III to oversee clinical trial operations and ensure compliance with protocols.
Posted by employer 3 days ago
First seen on Joblaze 2 days ago
Last verified on the company career page 7 hours ago
Not disclosed in this posting: compensation, years of experience, visa sponsorship.
Joblaze summary
The Clinical Research Associate III at CVRx oversees the daily operations of clinical trials, ensuring compliance with protocols and regulatory standards while monitoring trial sites. This role requires expertise in Good Clinical Practice and familiarity with clinical trial management, making it suitable for experienced professionals in the field. Candidates with a strong background in clinical research and the ability to travel frequently will find this position aligns with their skills. The role involves collaboration with the Clinical Study Manager and may require occasional on-site presence.
Quick facts
- Is the Clinical Research Associate (CRA) III (Hybrid) role remote?
- It's hybrid — CVRx expects some on-site time in Brooklyn Park, MN.
- Where is the role based?
- CVRx is hiring for this position in Brooklyn Park, MN.
- What seniority level is this role?
- CVRx targets mid-level candidates for this position.
- Is this full-time or contract?
- Full-time for this Clinical Research Associate (CRA) III (Hybrid) role at CVRx.
From the original posting
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.
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.
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.