Jobs at Cardiovascular Associates of America

Coordinates cardiovascular clinical trials, including patient recruitment, screening, enrollment, follow-up, data collection, documentation, sponsor communication, and regulatory compliance. Supports daily research site operations, maintains accurate clinical records and regulatory binders, ensures adherence to protocols and GCP/ICH guidelines, and contributes to workflow improvements. The role collaborates with investigators, sponsors, clinic staff, participants, and research stakeholders while managing studies independently in an onsite environment.

Coordinates cardiovascular clinical trials, including patient recruitment, screening, enrollment, follow-up, data collection, regulatory documentation, sponsor communication, and site operations. Ensures protocol compliance, accurate data entry, adherence to GCP and ICH guidelines, and timely reporting while supporting workflow improvements and collaborating with investigators, participants, and multidisciplinary staff.

Coordinates cardiovascular clinical trials, including participant recruitment, screening, enrollment, follow-up, data collection, documentation, sponsor communication, and regulatory compliance. Supports daily research-site operations, maintains regulatory records, ensures adherence to protocols and GCP/ICH requirements, and helps improve study workflows. The role requires collaboration with investigators, sponsors, clinic staff, participants, and research stakeholders.

Provides strategic in-house legal support focused on vendor, technology, professional services, and healthcare agreements. Drafts and negotiates contracts, manages the contract lifecycle, advises on healthcare regulatory and compliance matters, partners with executives on business risks, develops legal training, promotes CLM tools, and manages outside counsel. Requires a law degree, active state bar membership, and at least four years of legal experience.

Manage cardiovascular clinical trials from recruitment and enrollment through data collection, site operations, reporting, and regulatory compliance. Coordinate with sponsors, participants, clinic staff, and national research teams while maintaining accurate documentation and protocol adherence. Identify process improvements, support research program growth, and independently manage multiple study responsibilities in an on-site environment.

Supports clinical research site operations by scheduling participants, preparing visits, managing supplies, processing and shipping specimens, maintaining study logs and regulatory documents, and supporting investigational product accountability. Follows protocols, GCP, sponsor requirements, and site SOPs while escalating deviations and documentation concerns. The role is in-person in Schaumburg and requires confidentiality, organization, attention to detail, and coordination with study teams, laboratories, and couriers.

Provides psychosocial support and social determinants of health assessments for patients in a remote multidisciplinary care team. Develops care plans, coordinates referrals for behavioral health, financial, transportation, housing, food, and social services, and conducts follow-ups. Facilitates advance care planning discussions, documents patient interactions in EHR and care management systems, supports closed-loop referrals, and contributes to audits, reporting, quality improvement, and compliance activities.

Support enterprise cardiovascular quality initiatives by analyzing provider, practice, and network performance data; build and maintain dashboards and reports; identify variation and improvement opportunities; support audit readiness and documentation; collaborate with clinical leaders to drive quality improvement and present findings to stakeholders.

Coordinates cardiovascular clinical trials, including patient recruitment, screening, enrollment, follow-up, site operations, data management, sponsor communication, reporting, and regulatory documentation. Ensures compliance with study protocols, GCP, ICH guidelines, and applicable regulations while maintaining accurate records and identifying workflow improvements. Collaborates with investigators, sponsors, clinic staff, participants, and research stakeholders.

Coordinate and oversee cardiovascular clinical trials including patient recruitment, enrollment, follow-up, data collection and entry, regulatory compliance (GCP/ICH), site operations, sponsor communication, and process improvement to support study performance.

Seeking a full-time Cardiac Electrophysiologist to perform device implantation/management, AF ablations, lead extractions, cryoablation, Watchman procedures, and inpatient/outpatient EP consults. Work primarily at one campus with two dedicated EP labs, advanced 3D mapping (Carto, ESI), dedicated EP support, lucrative compensation, and a two-year partnership track with no buy-in.

Join a physician-led cardiovascular practice as a full-time Cardiac Electrophysiologist performing device implantation/management, AF ablations, lead extractions, cryoablation, Watchman procedures, and inpatient/outpatient EP consults. Work on one campus with two dedicated EP labs, advanced 3D mapping, a dedicated EP team, lucrative compensation, bonus, equity, and a two-year partnership track with no buy-in.

Provide comprehensive electrophysiology care across clinic, hospital, and ASC settings including diagnosis and treatment of arrhythmias, catheter ablations, device implantation/management, EP studies, mapping, remote monitoring, and potential structural heart procedures like Watchman.

Provide comprehensive electrophysiology care including diagnosis/treatment of arrhythmias, routine and complex catheter ablations, device implantation/management, EP studies, intracardiac mapping, remote monitoring, and inpatient/outpatient care. Collaborative practice with APPs and nurses, shared call, Monday–Friday schedule, opportunities for Watchman and structural heart procedures, with competitive compensation and partnership prospects.

Provide comprehensive electrophysiology care in clinic and hospital settings including diagnosis and management of arrhythmias, routine and complex catheter ablation, device implantation/management, EP studies, intracardiac mapping, remote monitoring, inpatient/outpatient care, and opportunities for structural heart procedures.

Perform CT and CTA exams using GE Optima 660 and AW workstation, produce high-quality images and reports, manage CT workflow and scheduling, perform basic X-rays, venipuncture and contrast administration, assist with ACR reaccreditation, equipment monitoring, patient prep and safety, and other department duties.

Provide comprehensive electrophysiology care across clinic and hospital settings: diagnose and treat arrhythmias, perform routine and complex catheter ablations, implant and manage cardiac devices, conduct EP studies and intracardiac mapping, manage remote monitoring and inpatient/outpatient EP care, and participate in related structural heart procedures.

Lead APP strategy and operations for a cardiology MSO: optimize APP utilization, standardize roles and workflows, design compensation models, support quality and value-based care initiatives, and partner with clinical and operations leaders to scale CVAUSA care models across inpatient and outpatient settings.

Provide operational and participant support for clinical studies: schedule visits, process and ship specimens, manage study supplies and documentation, maintain logs, support regulatory binders, and follow GCP/SOPs while assisting coordinators and investigators.

Coordinate and oversee cardiovascular clinical trials including recruitment, enrollment, data collection, and regulatory compliance. Manage site operations, maintain study documentation, communicate with sponsors and investigators, and support process improvements to enhance study performance.