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Clinical Site Liaison
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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.
