Senior Clinical Research Associate

Managing research activities at clinical sites, the full-time Senior Clinical Research Associate will oversee all stages of clinical studies, including site identification, study initiation visits, and compliance monitoring, while working remotely. Key responsibilities Manage research activities at participating clinical sites for various projects Conduct study initiation visits and ensure compliance with regulatory requirements Support site training on data collection and report safety-related events Required qualifications 5+ years of experience as a Clinical Research Associate 4-year university degree or Nursing Degree Experience in Oncology is required Proficiency in Microsoft Office, CTMS, and EDC Systems Ability to work independently with minimal supervision