
51 - 200 employees
Founded 2021
Headquartered in Orlando, Cardiovascular Associates of America aims to bring the best cardiovascular physicians in one network with the common mission of saving lives, reducing costs, and improving patient care through clinical innovation. Through CVAUSA’s physician-centered practice management model, physicians drive clinical care and their practice culture, while benefiting from the business expertise and shared resources available through CVAUSA.
🔥 10 minutes ago
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51 - 200 employees
Founded 2021
Headquartered in Orlando, Cardiovascular Associates of America aims to bring the best cardiovascular physicians in one network with the common mission of saving lives, reducing costs, and improving patient care through clinical innovation. Through CVAUSA’s physician-centered practice management model, physicians drive clinical care and their practice culture, while benefiting from the business expertise and shared resources available through CVAUSA.
• support daily use of REALTIME CTMS, eSource, and eRegulatory modules • assist users with system navigation, troubleshooting, and workflow questions • support implementation of new research technologies and sponsor systems • participate in system testing, validation, and workflow optimization activities • assist with user account management and access requests • develop and maintain protocol-specific eSource templates • translate study protocols into efficient electronic workflows • build visit-specific source documentation • configure forms, templates, workflows, and data collection tools • standardize eSource practices across research sites • evaluate coordinator workflows and identify opportunities for improvement • deliver training on REALTIME and research technology platforms • develop user guides, job aids, and training materials
• 3+ years of clinical research experience • experience as a CRC, Lead CRC, Research Manager, Regulatory Coordinator, or CTMS Administrator • experience using CTMS, EDC, eSource, eRegulatory, or sponsor systems • experience creating source documents and visit worksheets • understanding of clinical trial workflows from feasibility through study close-out • experience training research personnel preferred
• competitive salary • health insurance • flexible working hours • professional development opportunities • training on system administration • ongoing coaching and support
Apply Now🕒 February 26
Clinical Scientist/Senior supporting clinical development at Adverum Biotechnologies, a subsidiary of Eli Lilly. Responsibilities include study design, data generation and analysis in a contract role.
🇺🇸 United States – Remote
💵 $70 - $80 / hour
💰 $217M Post-IPO Equity on 2020-08
⏳ Contract/Temporary
🟠 Senior
🧪 Clinical Research
🦅 H1B Visa Sponsor
🕒 August 28, 2025
Clinical Research Nurse – Home Visits administers investigational products in patients' homes; supports protocol adherence.