Global Ophthalmology Clinical Research Lead – Remote

Trial Form Support; Teramo; A distancia; EUR 70.000 - 110.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Health insurance

Pension

Car allowance

Competitive compensation

Descripción de la vacante

Trial Form Support is seeking an experienced Clinical Research Manager (CRM) in Ophthalmology to lead clinical operations across studies and countries. The role ensures compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites.

The position offers home-based work in Poland, Spain, or Italy with exposure to cross-functional, internationally distributed teams. Responsibilities include managing day-to-day operations, serving as sponsor contact for operational

Formación

• 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.

Responsabilidades

• 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.

Conocimientos

Leadership

Communication

Problem-solving

ICH-GCP

Regulatory compliance

Monitoring & quality oversight

Descripción del empleo

Trial Form Support is seeking an experienced Clinical Research Manager (CRM) in Ophthalmology to lead clinical operations across studies and countries. The role ensures compliance with ICH-GCP, SOPs, and contracts while partnering with PMs, CRAs, sponsors, and sites.

The position offers home-based work in Poland, Spain, or Italy with exposure to cross-functional, internationally distributed teams. Responsibilities include managing day-to-day operations, serving as sponsor contact for operational