Clinical Research Associate – CRA

• Perform and coordinate clinical monitoring and site management activities
• Conduct remote and on-site visits to assess protocol and regulatory compliance
• Manage required clinical trial documentation and ensure audit readiness
• 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 SDR, SDV and CRF review
• Assess investigational product inventory and records
• Document observations in reports and letters
• Escalate deficiencies and follow issues through resolution
• Maintain contact with investigative sites between monitoring visits
• Conduct monitoring tasks according to the approved monitoring plan
• Participate in investigator payments and investigator meetings
• Identify potential investigators and initiate clinical trial sites
• Perform trial closeout and retrieve trial materials
• Ensure essential documents are complete and compliant with ICH-GCP and regulations
• Conduct on-site file reviews
• Track trial status and provide progress updates
• Maintain accurate and updated study systems, including Clinical Trial Management Systems
• Facilitate communication among investigative sites, the client company and internal project teams
• Respond to regulatory requirements, audits and inspections
• Complete expense reports and timesheets
• Contribute to project publications, tools and process improvement initiatives
• Travel more than 75%

• Bachelor's degree in a life sciences related field
• At least 1 year of clinical monitoring experience in a clinical environment, including clinical trials, medical terminology, medical research, clinical research or health care
• Alternatively, experience in a health sciences field with formal training in medical terminology and anatomy may be considered
• Valid driver's license where applicable
• Basic medical/therapeutic area knowledge and understanding of medical terminology
• Ability to attain and maintain working knowledge of ICH GCPs, applicable regulations and procedural documents
• Good oral and written communication skills
• Good interpersonal skills
• Customer focus, listening skills and attention to detail
• Good organizational and time management skills
• Flexibility and adaptability
• Well-developed critical thinking, root cause analysis and problem-solving skills
• Ability to manage Risk Based Monitoring concepts and processes
• Ability to work independently or in a team
• Solid knowledge of Microsoft Office and ability to learn appropriate software
• Good English and Hebrew language and grammar skills

• Competitive salary
• Extensive benefits package focused on employee health and well-being
• Flexible working culture
• Work-life balance
• Award-winning learning and development programme
• Professional and personal development opportunities
• Collaborative work environment
• Diverse, inclusive workplace valuing different experiences, backgrounds and perspectives