Clinical Research Associate (CRA) - Cardiovascular (Remote)

Responsibilities: The Clinical Research Associate (CRA) is responsible for performance and compliance for assigned protocols and sites, ensuring adherence to regulations and quality standards. They act as the primary site contact throughout all phases of a clinical research study and develop strong relationships with clinical sites.

Requirements: Candidates must have at least 5 years of relevant experience in healthcare, including 2 years of direct site management experience. An associate's degree or higher in a scientific or healthcare discipline is required.

Key skills: Clinical Research Methods, Clinical Site Management, Clinical Trials Monitoring, Data Analysis, Regulatory Compliance, Site Management, Pharmacovigilance, Good Documentation Practices, Adverse Event Reporting System, Clinical Trial Planning, Problem Solving Skills, Time Management, Organizational Skills, Interpersonal Skills, Conflict Management, Monitoring Skill

Keywords: Clinical Research, Clinical Trials, ICH/GCP, Site Monitoring Plan, Regulatory Documentation, Data Management, Clinical Operations, Site Selection, Monitoring Activities, Audit Activities, Patient Recruitment, Quality Standards, Adverse Event Reporting, CTMS, eTMF, Spanish Fluency