Remote Ophthalmology Clinical Research Manager

Trial Form Support; La Spezia; Remote; EUR 90,000 - 130,000; Full time

Benefits offered by this job

Competitive compensation

Health insurance

Pension

Car allowance where applicable

Job summary

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

This home-based role offers exposure to cross-functional, international teams and opportunities to advance innovative ophthalmic therapies and patient outcomes.

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.
• Provide guidance to CRAs on site challenges and escalations.
• Support recruitment and monitoring strategies to optimize study performance.
• Contribute to study communications and operational updates.
• Support business development initiatives, proposals, budget development, and bid defense activities.

Skills

Leadership

Communication

Problem-solving

ICH-GCP

Regulatory compliance

Monitoring and quality oversight

Project coordination

Tools

CTMS

Job description

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

This home-based role offers exposure to cross-functional, international teams and opportunities to advance innovative ophthalmic therapies and patient outcomes.