Senior Clinical Research Associate

About this role

<div class="content-intro"><p style="margin: 0in; text-align: justify; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 10.0pt; font-family: Arial, sans-serif;">AtriCure, Inc. provides innovative technologies for the treatment of Afib and related conditions. Afib affects more than 33 million people worldwide. Electrophysiologists and cardiothoracic surgeons around the globe use AtriCure technologies for the treatment of Afib and reduction of Afib related complications. 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. AtriCure’s Hybrid AF™ Therapy is a minimally invasive procedure that provides a lasting solution for long-standing persistent Afib patients. AtriCure’s cryoICE cryoSPHERE® probe is cleared for temporary ablation of peripheral nerves to block pain, providing pain relief in cardiac and thoracic procedures. For more information, visit AtriCure.com or follow us on Twitter @AtriCure.</span></p> <p style="margin: 0in; text-align: justify; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"> </p> <p style="margin: 0in; text-align: justify; line-height: normal; font-size: 12pt; font-family: Aptos, sans-serif;"><span style="font-size: 10.0pt; font-family: Arial, sans-serif;">We foster a culture of inclusion by embracing diverse experiences and individuals where everyone’s authentic self is welcome. We offer supporting programs and resources that provide enriching and equitable opportunities for each person to contribute professionally and personally.</span></p></div><p></p> <p style="margin: 0in 20.7pt 0.0001pt 13.5pt; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"><span style="font-size: 10.0pt; color: black;">POSITION SUMMARY:</span></p> <p style="margin: 0in 20.7pt 0.0001pt 13.5pt; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"><span style="font-size: 10.0pt; color: black; ">The Senior Clinical Research Associate (Sr. CRA) at AtriCure plays a vital role in the Clinical Affairs department, independently managing and overseeing site management and/or monitoring activities during clinical trial execution. This position requires a high level of autonomy and leadership, providing guidance to junior team members and ensuring compliance with regulatory standards and protocols. The Sr. CRA is instrumental in maintaining the integrity of clinical data and adapting to evolving study needs.</span></p> <p style="margin: 0in 20.7pt 0.0001pt 13.5pt; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"> </p> <p style="margin: 0in 20.9pt 0.0001pt 13.5pt; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"><span style="font-size: 10.0pt; color: black; ">ESSENTIAL FUNCTIONS OF THE POSITION:</span></p> <p style="margin: 0in 20.9pt 0.0001pt 13.5pt; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"><span style="font-size: 10.0pt; color: black; ">Site Management</span></p> <ul style="margin-top: 0in; margin-bottom: .0001pt;"> <li style="margin: 0in 20.7pt 0.0001pt 0px; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"><span style="font-size: 10.0pt; color: black;">Coordinate the collection and review of essential documents from clinical investigation sites in collaboration with study team personnel.</span></li> <li style="margin: 0in 20.7pt 0.0001pt 0px; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"><span style="font-size: 10.0pt; color: black;">Conduct Site Qualification, Initiation, Interim and Close-Out training visits.</span></li> <li style="margin: 0in 20.7pt 0.0001pt 0px; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"><span style="font-size: 10.0pt; color: black;">Facilitate required training sessions (e.g., EDC, Protocol, Device) and support site nomination and qualification processes.</span></li> </ul> <p style="margin: 0in 20.7pt 0.0001pt 13.5pt; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"> </p> <p style="margin: 0in 20.9pt 0.0001pt 13.5pt; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"><span style="font-size: 10.0pt; color: black; ">Site Communications</span></p> <ul style="margin-top: 0in; margin-bottom: .0001pt;"> <li style="margin: 0in 20.7pt 0.0001pt 0px; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"><span style="font-size: 10.0pt; color: black;">Act as the primary point of contact for site communications and inquiries.</span></li> <li style="margin: 0in 20.7pt 0.0001pt 0px; text-align: justify; line-height: normal; font-size: 11pt; font-family: Arial, sans-serif;"><span style="font-size: 10.0pt; color: black;">Liaise with clinical study management, field personnel, and CROs, addressing moderately complex protocol or study related issues as…