Research Analyst

• Conduct site monitoring responsibilities for clinical trials
• Provide oversight, leadership, and guidance in the management and execution of clinical trials to ensure compliance and quality
• Ensure appropriate and timely investigator site visits
• Provide guidance, oversight, and feedback to the CRA team to ensure adherence to project scope, SOPs, timelines, and budget requirements
• Review monitoring visit reports, conduct co-monitoring and evaluation visits as needed
• Prepare consistently accurate and timely monitoring visit reports documenting site-related problems, resolutions, actions taken, protocol deviations, study progress, and enrollment status
• Participate in internal, client/sponsor, scientific, and other meetings as required

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Senior Clinical Research Associate