Medical Monitor

Responsibilities:

• 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 with regard to protocol
• Attend drug safety meetings/ external meetings
• Patient eligibility review
• Review AE/ SAEs
• Protocol training to site staff, CRAs etc
• Attend, participate/ present in investigator meetings

Qualification: MBBS/ MD qualification 

Eligibility:

• 3 year+ of clinical trial experience
• Familiar with clinical trials operations
• Good English communication skills
• Proficiency in using Microsoft office