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

As Clinical Research Manager (CRM) in Ophthalmology, you lead clinical operations across multiple studies and countries. You will ensure compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites. This role focuses on delivering trials on time, in scope, and to high quality, within a global CRO environment. Your work helps advance innovative ophthalmic therapies and improve patient outcomes. The position offers home-based work in Poland, Spain, or Italy and exposure to cross-functional, internationally distributed teams.

• competitive compensation
• health insurance
• pension
• car allowance where applicable
• 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
• 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
• leadership
• communication
• problem-solving
• ICH-GCP
• regulatory compliance
• monitoring and quality oversight