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'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 (Argentina)
🏢 Safeguard Global
📍 Argentina