Remote Ophthalmology Clinical Research Manager

Trial Form Support; Vicenza; Remote; EUR 70,000 - 110,000; Full time

Benefits offered by this job

Health insurance

Pension

Car allowance where applicable

Competitive compensation

Job summary

Trial Form Support is seeking a Clinical Research Manager (CRM) in Ophthalmology to lead clinical operations across studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites in a global CRO environment.

The role is home-based with potential in Europe. You will guide CRAs, monitor site quality, develop monitoring plans, and support recruitment and study performance, contributing to innovative ophthalmic therapies and

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 clinical trial processes from startup through closeout.
• In-depth knowledge 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.
• Review CTMS data for accurate country/site/subject information.
• Collaborate on CRA onboarding, training, and handover with Project Managers.
• Contribute to study communications and operational updates.
• Offer insights on resource utilization, revenue recognition, and forecasting.
• Participate in Investigator Meetings and present monitoring requirements when required.
• Promote proactive issue resolution and a solution-oriented approach.
• Support business development initiatives, proposals, budget development, and bid defense activities as required.

Skills

Leadership

Communication

Problem solving

ICH-GCP

Regulatory compliance

Monitoring oversight

Tools

CTMS

Job description

Trial Form Support is seeking a Clinical Research Manager (CRM) in Ophthalmology to lead clinical operations across studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites in a global CRO environment.

The role is home-based with potential in Europe. You will guide CRAs, monitor site quality, develop monitoring plans, and support recruitment and study performance, contributing to innovative ophthalmic therapies and