Clinical Research Coordinator I
Core
Coordinate patient management and execution of clinical studies in cardiology, including recruitment, data management, and regulatory submissions.
Role type
Clinical Research Coordinator I (IC)
Builds
Clinical trial data and patient study visits
Domain
Healthcare / Clinical Research / Cardiology
Required skills
Clinical trial protocol execution, participant recruitment and screening, informed consent processes, data entry and management, regulatory compliance (ICH/GCP), budgeting oversight, report preparation, liaison with sponsors and ethics boards
Preferred skills
Cardiology research experience, ACRP/SoCRA certification (CCRP), TDG certification, IATA shipping regulations knowledge, investigational product development knowledge
Technologies
MS Office (Outlook, Word, Excel, PowerPoint), CRFs
Responsibilities
Recruit and screen study participants; Execute patient study visits per protocol; Manage data collection and entry; Review study documents; Contribute to budgeting; Prepare status reports; Submit to ethics boards; Liaise with stakeholders
Seniority
Mid-level, hands-on IC