Global Site Activation Specialist – Clinical Trials

IQVIA; Madrid; Presencial; EUR 40.000 - 56.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Global team

Diverse studies

Innovative technologies

Career growth

Descripción de la vacante

IQVIA is seeking a Site Activation Specialist in Spain to act as a single point of contact for feasibility, site activation and maintenance across assigned studies. You will review regulatory documents, coordinate with Site Activation Manager and project teams, and ensure accurate updates to timelines and systems.

This role demands independent work, strong collaboration, and meticulous attention to regulatory details.

Formación

• Bachelor’s Degree in Life Science or related field.
• Minimum of 3 years’ experience in Clinical Research.
• Experience with Ethics Committees and Regulatory Authorities submissions.
• Familiarity with site activation processes.
• Knowledge of regulatory requirements and ICH/ GCP

Responsabilidades

• Serve as a Single Point of Contact for feasibility, site activation, and maintenance.
• Review documents for completeness and accuracy under guidance.
• Prepare site documents and inform team upon completion.
• Update databases, timelines, and project plans with accurate information.

Conocimientos

Independent work

Collaboration

Interpersonal skills

Organisational skills

Multitasking

Communication

Project coordination

Educación

Bachelor’s Degree in Life Science or related field

Descripción del empleo

IQVIA is seeking a Site Activation Specialist in Spain to act as a single point of contact for feasibility, site activation and maintenance across assigned studies. You will review regulatory documents, coordinate with Site Activation Manager and project teams, and ensure accurate updates to timelines and systems.

This role demands independent work, strong collaboration, and meticulous attention to regulatory details.