Valencia: Part-Time Clinical Research Coordinator

Icon; Alcobendas; Presencial; EUR 20.000 - 26.000; A tiempo parcial

Ventajas ofrecidas por este puesto de trabajo

Annual leave

Health insurance offerings

Retirement planning options

Global EAP Lifeworks 24/7 assistance

Life assurance

Country-specific benefits

Descripción de la vacante

ICON Plc in Valencia, Spain, is seeking a Clinical Research Coordinator for a part-time 50% FTE position. You will coordinate day-to-day trial activities, ensure regulatory compliance, and support site staff to drive efficient trial execution.

The role requires a strong foundation in clinical coordination, experience with trial processes, and excellent communication within diverse teams. Join ICON to support patients and advances in clinical research.

Formación

• Bachelor's degree in a relevant scientific discipline or healthcare-related field.
• Extensive experience as a Clinical Research Coordinator with understanding of trial processes and regulatory requirements.
• Strong organizational and multitasking skills to manage multiple trial aspects.
• Proficiency in clinical trial software and data management with attention to detail.
• Excellent communication and teamwork skills for diverse study teams.

Responsabilidades

• Coordinate and manage day-to-day activities of clinical trials to ensure efficient execution.
• Ensure adherence to study protocols, regulatory requirements, and GCP standards.
• Monitor and document trial progress, including data collection and safety reporting.
• Provide training and support to site staff to ensure proper trial procedures.
• Build and maintain relationships with study participants and site personnel.

Conocimientos

Clinical coordination

Regulatory knowledge

Multitasking

Communication skills

Team collaboration

Educación

Bachelor's degree in a relevant scientific discipline or healthcare-related field

Herramientas

Clinical trial software

Descripción del empleo

ICON Plc in Valencia, Spain, is seeking a Clinical Research Coordinator for a part-time 50% FTE position. You will coordinate day-to-day trial activities, ensure regulatory compliance, and support site staff to drive efficient trial execution.

The role requires a strong foundation in clinical coordination, experience with trial processes, and excellent communication within diverse teams. Join ICON to support patients and advances in clinical research.