Senior Clinical Trial Coordinator: Lead Global Trial Support

ThermoFisher Scientific; España; Presencial; EUR 42.000 - 66.000; Jornada completa

Descripción de la vacante

Thermo Fisher Scientific is seeking a Senior Clinical Trial Coordinator to provide administrative and technical support to the Project Team in Spain. You will coordinate activities and may serve as a study lead, acting as a cross-functional liaison to ensure trials progress smoothly.

Strong organizational skills, MS Office proficiency and experience with clinical trial systems (GoBalto, eTMF) are required. You will assist training, process improvements and regulatory documentation throughout the

Formación

• Strong teamwork and communication across cross-functional teams.
• Experience coordinating clinical trials and managing study timelines.
• Knowledge of ICH GMP, regulatory requirements and SOPs.
• Proficiency with MS Office and trial databases.
• Ability to train staff and share best practices.

Responsabilidades

• Coordinate and oversee trial activities as per task matrix.
• Perform department, country and investigator file reviews and document findings.
• Ensure tasks are on time and within budget; communicate risks to leads.
• Maintain study documentation and support systems (GoBalto, eTMF).
• Support RBM activities and schedule client/internal meetings.

Conocimientos

Teamwork

Organizational skills

Data analysis

Customer focus

Flexibility

Regulatory knowledge

English proficiency

Presentation skills

MS Office

Clinical trial systems

Educación

Bachelor's degree preferred

High school diploma

Clinical trial experience

Herramientas

GoBalto

eTMF

Clinical trial databases

Descripción del empleo

Thermo Fisher Scientific is seeking a Senior Clinical Trial Coordinator to provide administrative and technical support to the Project Team in Spain. You will coordinate activities and may serve as a study lead, acting as a cross-functional liaison to ensure trials progress smoothly.

Strong organizational skills, MS Office proficiency and experience with clinical trial systems (GoBalto, eTMF) are required. You will assist training, process improvements and regulatory documentation throughout the