Research Analyst

• Develop and conduct site training on protocol requirements, source documentation completion, and electronic data capture (EDC).
• Conduct regular site monitoring visits (virtually and physically) and prepare reports for study initiation, monitoring, and close-out visits.
• Ensure site adherence to study protocols and regulatory requirements.
• Draft and/or provide input into Clinical Study Protocols, supporting plans and procedures, including Informed Consent Forms (ICFs), Monitoring Plans and Data Collection Forms in conjunction with the assigned Project Team.
• Assist with Institutional Review Board (IRB) management.
• Manage study budget and agreements with study sites.
• Manage study Trial Master Files.
• Serve as primary point of contact with study sites.
• Monitor and analyze clinical study data and report on performance to the project team.
• Assist with the development of study databases for managing clinical data.

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