Clinical Research Associate I

• Monitor investigator sites using a risk-based monitoring approach
• Apply root cause analysis, critical thinking, and problem-solving to identify site process failures and corrective/preventive actions
• Ensure data accuracy through source document review, source data verification, and case report form review during on-site and remote monitoring
• Assess investigational products through physical inventory and records review
• Document observations in reports and letters using approved business-writing standards
• Escalate deficiencies and issues to clinical management and follow them through resolution
• Maintain contact with investigative sites between monitoring visits to confirm protocol compliance, issue resolution, and timely data recording
• Conduct monitoring tasks according to the approved monitoring plan
• Participate in investigator payment processes and investigator meetings
• Identify potential investigators and initiate clinical trial sites according to applicable procedures, protocols, regulations, and ICH GCP obligations
• Perform trial closeout and retrieve trial materials
• Ensure essential documents are complete and maintained according to ICH-GCP and applicable regulations
• Conduct on-site file reviews according to project specifications
• Provide trial status tracking and progress reports
• Maintain accurate and current study systems, including Clinical Trial Management Systems
• Facilitate communication among investigative sites, the client company, and internal project teams
• Respond to company, client, and regulatory requirements, audits, and inspections
• Complete administrative tasks such as expense reports and timesheets
• Assist with project publications and tools, share suggestions, and contribute to process-improvement initiatives

• Bachelor's degree in a life sciences-related field, or Registered Nursing certification, or equivalent formal academic/vocational qualification
• Minimal clinical monitoring experience comparable to 2 years
• Experience in a clinical environment involving clinical trials, medical terminology, medical research, clinical research, health care, or a health sciences field with formal training in medical terminology
• Ability to comply with sponsor/client/site requirements, including possible disclosure of vaccination status or other personal information
• Ability to travel frequently, generally 60–80%, with a stated requirement higher than 75%
• Ability to drive frequently to site locations
• Ability to work in office, laboratory, clinical, and/or home-office environments
• Ability to use required personal protective equipment, including protective eyewear, garments, and gloves
• Ability to tolerate possible exposure to biological fluids, infectious organisms, electrical office equipment, and fluctuating or extreme temperatures

• Fully remote work mode
• Standard Monday–Friday work schedule