Are you a Clinical Research Manager with hands-on ophthalmology trial experience looking to lead at country and site level on cutting-edge retina studies? This role is for someone who already owns CRM delivery end-to-end and wants to do it within a specialized, passionate ophthalmology team. Before you apply — this is a dedicated ophthalmology role We're looking specifically for candidates with direct retina/ophthalmology trial experience and proven independent CRM ownership.

If that's you, we'd love to talk .

What you'll doYou coordinate and oversee country and site management activities throughout study conduct, ensuring high-quality delivery aligned to SOPs, ICH/GCP, and regulatory requirements. Day to day, you wil - l:

Own clinical operations delivery against protocol, SOPs, and regulatory standa - rdsServe as the primary operational point of contact for Spons - orsLead, train, and supervise CRAs, including co-monitoring and review of visit repo - rtsDrive site and country performance:



monitoring oversight, protocol deviations, recruitment, and issue escalat - ionMaintain oversight of TMF quality, CTMS accuracy, and study documentat - ionPartner with the Project Manager on planning, investigator payments, resourcing, and forecast - ingContribute to Investigator Meetings, feasibility, and start-up ("greenlight") activit ies

What you need (the non-negotiab - les)Minimum 5 years of clinical monitoring experience (CRO, pharma, or biot - ech)At least 1 year as a CRM with proven, independent oversight of site and country operat - ionsDirect ophthalmology trial experience, ideally in retina indications (DME, AMD, GA, RVO, or I - RDs)Full-lifecycle study exposure, including start-up / activation experi - enceFull English Profici - encyStrong command of ICH/GCP and clinical operations proce

📌 Clinical Research Manager (CRM) — Ophthalmology (Retina)
🏢 Safeguard Global
📍 Argentina