Global Feasibility Specialist – Clinical Trials

IQVIA; Madrid; Presencial; EUR 60.000 - 90.000; Jornada completa

Descripción de la vacante

IQVIA is seeking a Global Feasibility Specialist to support clinical systems and tools used by Development Operations. You will work with study teams to identify sites, set up feasibility processes, and provide data-driven inputs to optimize site selection for clinical studies.

In this role, you will analyze data, coordinate with stakeholders, and stay current with regulatory trends. The position emphasizes collaboration, system setup, and ongoing feasibility activities across multiple

Formación

• Bachelor's degree in a scientific or allied health field with 3+ years of clinical trial experience and/or 2+ years in feasibility/recruitment.
• Experience with trial optimization vendors, tools, and methods.
• Ability to prioritize multiple projects within tight timelines.
• Experience working in multiple rare disease therapeutic areas.
• Experience with data analysis and interpretation.
• Highly proficient with Excel.

Responsabilidades

• Work with clinical study teams to ensure CTMS data accuracy.
• Provide user support for clinical systems, handling issue/enhancement requests.
• Identify potential sites that meet study criteria through research and data analysis.
• Assist with feasibility launch including system setup and outreach for site-level questionnaires.
• Communicate with study teams and stakeholders to coordinate feasibility activities.
• Track feasibility responses and report to internal stakeholders.
• Troubleshoot issues in the feasibility process.
• Stay updated on regulations and trends related to site feasibility.
• Support enrollment forecasting and discuss scenarios with stakeholders.

Conocimientos

Data analysis

Prioritization

Rare disease experience

Excel proficiency

Educación

B.S. in a scientific or allied health field

Herramientas

Trial optimization tools

Descripción del empleo

IQVIA is seeking a Global Feasibility Specialist to support clinical systems and tools used by Development Operations. You will work with study teams to identify sites, set up feasibility processes, and provide data-driven inputs to optimize site selection for clinical studies.

In this role, you will analyze data, coordinate with stakeholders, and stay current with regulatory trends. The position emphasizes collaboration, system setup, and ongoing feasibility activities across multiple