Senior Clinical Trial Coordinator — Hybrid Role in Lisbon

Thermo Fisher Scientific Inc.; Lisboa; Híbrido; EUR 35 000 - 52 000; Tempo integral

Resumo da oferta

Thermo Fisher Scientific Inc. in Lisbon, Portugal, seeks a Senior Clinical Trial Coordinator to provide administrative and technical support to the Project Team in a hybrid or office environment.

You will coordinate trial activities, manage regulatory documents, and assist with process improvements within the clinical operations landscape. The role requires a strong background in clinical trials, excellent English and local language skills, and the ability to train staff and onboard new team

Qualificações

• High/Secondary school diploma or equivalent with relevant formal qualification.
• Bachelor's degree is preferred for this role.
• 4+ years of relevant experience or equivalent combination of education and experience.
• Equivalent combinations of education, training and/or experience may be considered.

Responsabilidades

• Coordinate trial activities and support project teams in a cross-functional role.
• Review and document regulatory and study-related materials to ensure compliance.
• Maintain study documentation and provide training support as needed.
• Assist with meetings, minutes, and tracking of study metrics and actions.
• Support information systems including GoBalto and eTMF for trial management.

Conhecimentos

Teamwork

Organization

Communication

English proficiency

MS Office

Project coordination

Attention to detail

Formação académica

High/Secondary school diploma or equivalent

Bachelor's degree preferred

Ferramentas

GoBalto

eTMF

MS Office

Descrição da oferta de emprego

Thermo Fisher Scientific Inc. in Lisbon, Portugal, seeks a Senior Clinical Trial Coordinator to provide administrative and technical support to the Project Team in a hybrid or office environment.

You will coordinate trial activities, manage regulatory documents, and assist with process improvements within the clinical operations landscape. The role requires a strong background in clinical trials, excellent English and local language skills, and the ability to train staff and onboard new team