Remote Global Ophthalmology Clinical Research Manager

Trial Form Support; Prato; Remote; EUR 90,000 - 120,000; Full time

Job summary

Trial Form Support seeks a Clinical Research Manager (CRM) in Ophthalmology to lead clinical operations across multiple studies and countries within a global CRO setting.

You will ensure ICH-GCP and contracts compliance while partnering with PMs, CRAs, sponsors, and sites, delivering trials on time, in scope, and to high quality. This home-based role spans Poland, Spain, and Italy, with exposure to cross-functional teams.

Qualifications

• Minimum 5 years in clinical research with substantial on-site monitoring experience as a CRA.
• At least 1 year as an Unmasked CRA/CRM in an Ophthalmology study.
• Experience coordinating or overseeing clinical trial operations at study, country, or regional level.
• Strong understanding of ICH-GCP, regulatory requirements, and clinical research standards.

Responsibilities

• Manage day-to-day clinical operations for assigned projects per protocol, contracts, and regulatory requirements.
• Serve as primary sponsor contact for operational issues and study deliverables.
• Lead and coach CRAs, ensuring completion of training requirements.
• Oversee site quality and monitoring deliverables through direct supervision.
• Develop and implement monitoring plans, site training plans, and verification initiatives.
• Coordinate investigator meetings and country/site level reporting.
• Ensure practical, effective study processes from feasibility to closeout.
• Provide guidance to CRAs on site challenges and escalations.
• Support recruitment and monitoring strategies to optimize study performance.
• Conduct co-monitoring visits and review monitoring reports for timely issue resolution.

Skills

Leadership

Communication

Problem solving

ICH-GCP

Regulatory compliance

Monitoring & quality oversight

Tools

CTMS

Job description

Trial Form Support seeks a Clinical Research Manager (CRM) in Ophthalmology to lead clinical operations across multiple studies and countries within a global CRO setting.

You will ensure ICH-GCP and contracts compliance while partnering with PMs, CRAs, sponsors, and sites, delivering trials on time, in scope, and to high quality. This home-based role spans Poland, Spain, and Italy, with exposure to cross-functional teams.