Clinical Research

• Conduct and report all types of onsite monitoring visits
• Be involved in study startup
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Serve as a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Participate in feasibility research
• Support the regulatory team in preparing documents for study submissions
• Support and participate in audits and inspections

Clinical Research jobs in Bosnia and Herzegovina

Clinical Research Associate