• Performs site qualification, site initiation, interim monitoring, site management and close-out visits (performed on-site or remotely) ensuring regulatory, ICH-GCP and/or Good Pharmacoepidemiology Practice (GPP) and protocol compliance. • Uses judgment and experience to evaluate overall performance of site and site staff and to provide recommendations regarding site-specific actions; immediately communicates/escalates serious issues to the project team and develops action plans. • Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance, relevant regulations, and company SOPs/processes. • Verifies the process of obtaining informed consent has been adequately performed and documented for each subject/patient as required/appropriate. • Demonstrates diligence in protecting the confidentiality of each subject/patient.

• Monitoring clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards • Conducting site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution • Collaborating with cross-functional teams to ensure timely and accurate data collection and reporting • Providing training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct • Building and maintaining effective relationships with site personnel and stakeholders to facilitate smooth trial operations

• Research and qualify artists based on social engagement rates (minimum of 2%) and upcoming tour schedules. • Draft and send outreach emails to potential artist partners, utilizing proven templates and following best practices. • Review and verify artist tour schedules to ensure timely and relevant follow-up. • Support the partnership team in managing the artist pipeline, ensuring that no leads fall through the cracks. • Assist in identifying new potential leads and opportunities for partnership growth. • Maintain accurate tracking of outreach and responses, improving the process for scalability.

Role Description 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 sites. The CRA II will assist with the implementation and execution of study protocols and associated study documents for clinical trials, including clinical monitoring of AtriCure studies. This also includes the coordination of site activities from site start-up to site closure as needed. The CRA II will work closely with the Clinical Project Managers and Sr. CRAs to ensure the study is executed to meet project deliverables. The CRA II will be responsible for the study start-up process for AtriCure’s Clinical Investigational protocols, which includes but is not limited to: - Protocol review - Informed Consent Development - CRF design - EDC testing - Preparation of site-specific logs/documentation and investigator study files The CRA II will participate as needed in study review meetings and attend scientific meetings and industry conferences as required. The CRA II will also conduct site visits including: - Site Qualification Visits - Site Initiation Visits - Interim Monitoring Visits - Close Out Visits Qualifications - Bachelor’s degree in a science or related technical field required or demonstrated equivalent combination of education, training and experience - Minimum two years of CRA experience - Comprehensive knowledge of ISO, GCP, ICH, FDA and other applicable regulations governing the conduct of clinical trials - Ability to manage role/responsibility independently - Recognize problems, trends and react to resolve issues quickly and to bring effective resolution - Experience working with electronic data capture systems - Strong attention to detail and an ability to prioritize and juggle multiple/competing issues - Ability to create and manage key internal and external partnerships - Excellent written and verbal communication skills - Experienced user of Microsoft Office software including WORD, Excel, and PowerPoint - Ability to travel up to 50% Requirements - Assist Clinical Project Managers and Sr. CRAs in the study development and start-up process development of the informed consent form and internal review prior to submission to the IRB/EC - Collection of startup documentation from clinical investigational site - Verify that the investigator and research staff follow the approved protocol and all GCP procedures - Conduct weekly maintenance and management of study sites to ensure site compliance with study protocol, GCP/ICH, and applicable regulations - Conduct initial and ongoing study training of site personnel throughout the clinical study - Monitor and report to ATRC site enrollment activities - Verify that all research staff and facilities have adequate resources and qualifications and are maintained throughout the course of the study - 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 and ensure corrective action is implemented - Review queries and assist in the resolution of DCFs - Participate in project team meetings - Participate in departmental development initiatives (e.g. training, SOP development/updates, etc.) - Ability to work on multiple projects as departmental priorities change Benefits - Medical & Dental beginning day 1 of employment - 401K plus match - 30 days of paid Parental Leave, in addition to maternity leave, for new moms and dads - Volunteer Time off - Pet Insurance - Access to on-site fitness center and cafeteria for corporate-based employees