
Clinical Site Liaison
Há 14 horas
Job Title: Clinical Site Liaison Type: Contract (12 months)
Location: Latin America
Responsibilities:
Oversight of site management activities, CRO monitors, patient recruitment and engagement with PI's and site staff.
Act as the primary regional contact for CRA, site coordinators and investigative sites, ensuring a high level of engagement and performance throughout the study lifecycle.
Focus on study execution and operational excellence across multiple clinical studies and regions.
Support site identification, monitoring, supplies, feasibility, initiation, and activation activities in collaboration with the global study team.
Provide operational guidance and hands-on support to ensure timely patient recruitment and high-quality data collection.
Monitor site performance metrics (recruitment, data entry, protocol compliance) and proactively identify and address performance issues.
Participate in site visits or virtual meetings as needed to support inspection readiness and resolve site-specific challenges.
Ensure site adherence to study protocols, ICH-GCP, SOPs, and applicable regulatory requirements.
Provide CRA oversight during site monitoring visits
Qualifications:
Bachelor’s degree in life sciences, nursing, pharmacy, or a related field
5+ years of experience in clinical research, with at least 2 years in a site-facing or monitoring role (CRA, Site Manager, or Clinical Trial Liaison experience advantageous).
Must have strong experience with Ophthalmology and Neurology.
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