Research Analyst

• Oversee and manage clinical trial sites, ensuring that studies are conducted in accordance with regulatory requirements, study protocols, and company standards.
• Coordinate clinical trial monitoring delivery, resolving issues, and developing team capability.
• Lead and oversee site management activities, including site selection, initiation, monitoring, and close-out visits, ensuring compliance with study protocols, SOPs, ICH-GCP, and applicable regulatory requirements.
• Serve as the primary point of contact for the sponsor, ICON CRAs, and clinical sites, providing effective communication, resolving site-level issues, and maintaining strong site relationships to support study success.
• Provide ongoing oversight of study progress through regular review of study metrics, KPIs, risks, and escalations.
• Support and guide the CRA team by reviewing monitoring reports, providing regular feedback, and conducting co-monitoring visits as needed.
• Work closely with the Study Manager to ensure alignment on study timelines, deliverables, and quality expectations, contributing to high-quality trial execution.
• Oversee and support CRA responsibilities related to site performance and subject recruitment.
• Monitor KPIs and metrics to ensure performance is within expectations, set clear site expectations, and follow up on timely and effective action plans.
• Mentor and develop CRAs, supporting their professional growth and promoting consistent application of best practices across studies.

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