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Clinical Research Associate II
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- Clinical Research Associate II Cincinnati, OH, USA ● Mason, OH, USA ● Minneapolis, MN, USA ● Minnetonka, MN, USA Req #2009 Monday, April 1, 2024 AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions.
- AtriCure’s Isolator Synergy Ablation System is the first medical device to receive FDA approval for the treatment of persistent Afib. AtriCure’s AtriClip Left Atrial Appendage Exclusion System products are the most widely sold LAA management devices worldwide.
- POSITION SUMMARY:The Clinical Research Associate II (CRA II) will be a key contributor to AtriCure’s clinical affairs department and primarily responsible for the site management of assigned clinical investigative CRA II will assist with the implementation and execution of study protocols and associated study documents for clinical trials, includingclinical monitoring of AtriCure also includes the coordination of site activities from site start-up to site closure as needed.
- The CRA II will be responsible for the study start up process for AtriCure’s Clinical Investigational protocols, which includes and is not limited to the following: protocol review, Informed Consent Development, CRF design, EDC testing, preparation of site-specific logs/documentation and investigator study files.
- Assist with the preparation of clinical study devices and verify the accountability of investigational devices are properly received, tracked, and secured at the study site Ensure adverse events, concomitant medications, and inter-current illnesses are reported in accordance with the protocol on the CRF. Communicate deviations from the protocol, SOPs, GCP, and applicable regulatory requirements to the investigator andensure corrective action is implemented.
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