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

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What you'll doYou'll 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

sses

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