Sr. Clinical Research Associate (CRA)- Early Stage Development (ESD) Remote

Responsibilities: The role is accountable for performance and compliance for assigned protocols and sites, ensuring adherence to ICH/GCP and country regulations. The CRA acts as the primary site contact and manager throughout all phases of a clinical research study.

Requirements: Candidates must have early stage development experience and at least 7 years of relevant experience in healthcare, including 4 years of direct site management experience. An associate's degree or bachelor's degree in a scientific or healthcare discipline is required.

Key skills: Adverse Event Report, Biopharmaceutics, Clinical Data Management, Clinical Development, Clinical Research, Clinical Study Management, Clinical Trial Documentation, Clinical Trial Management, Clinical Trials Monitoring, Customer-Focused, Early Clinical Development, Preventive Action, Regulatory Affairs Compliance, Site Management

Keywords: Clinical Research Associate, Early Stage Development, ICH, GCP, Site Management, Monitoring, Clinical Trials, Regulatory Documentation, Data Management, Patient Recruitment, Quality Control, Audit, Inspection, Clinical Trial Planning, Clinical Trial Management System, Electronic Trial Master File