Medical Monitor
Contract role
Budapest Hungary Description
• Review protocol and provide suggestions
• Respond to queries/ clarifications from EC/ IRBs
• Answer medical questions from sites or project team
• Respond to queries from sites about protocol
• Attend drug safety meetings/ external meetings (e.g. IDMCs)
• Review protocol and provide suggestions
• Respond to queries/ clarifications from EC/ IRBs
• Answer medical questions from sites or project team
• Respond to queries from sites about protocol
• Attend drug safety meetings/ external meetings (e.g. IDMCs)
• Patient eligibility review
• Review AE/ SAEs
• Protocol training to site staff, CRAs, investigators, etc.
• Attend, participate/ present in investigator meetings
Basic Qualification and experience:
• MBBS/ MD qualification
• Min 3 years of experience of working in clinical research
• Familiar with clinical trials operations, EDC, data review and visualization tools...