Global Feasibility Specialist - Spain

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

Job Summary

The Global Feasibility Specialist supports the administration of the clinical systems and tools utilized by Development Operations. Works in close collaboration with Development Operations teams, study start-up to provide key inputs, metrics, and outputs to support the selection of the most suitable sites for our clinical studies.

Summary Of The Essential Functions Of The Job

• Work with clinical study teams to ensure the accuracy of data in CTMS
• Provide support, under the direction of the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist, to clinical systems end users, including receipt, evaluation and recommendation for all issue/enhancement requests
• Conduct research and data analysis to identify potential sites that meet the study criteria and objectives
• Assist with feasibility launch to include system set-up, feasibility questionnaire creation and site-level feasibility questionnaire outreach
• Effectively communicating with study teams and relevant stakeholders as needed to coordinate and support additional feasibility activities as identified by the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist
• Tracking and data entry of feasibility responses and reporting responses to the internal stakeholders
• Troubleshoot any issues or discrepancies that arise in the feasibility process (in-house and/or outsourced studies)
• Stay up to date with current regulations and industry trends related to site feasibility
• Supporting enrollment forecasting and discussing scenarios with internal or external stakeholders under the supervision of the Global Site Identification and Feasibility Manager or Senior Global Site Identification and Feasibility Specialist

Minimum Requirements

• B.S. in a scientific or allied health field (or equivalent degree) and 3+ years of experience demonstrating thorough understanding of clinical trial conduct and processes and/or 2+ years of feasibility/recruitment
• Experience with trial optimization vendors, tools, and methods
• Ability to prioritize multiple projects and tasks within tight timelines
• Experience working in multiple rare disease therapeutic areas
• Experience with data analysis and interpretation
• Highly proficient with excel

IQVIA is a leading global provider of clinical research services, commercial insights, and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com.

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

At IQVIA, we believe that diversity, inclusion, and belonging empower our mission to accelerate innovation for a healthier world. We create a culture of belonging by valuing the perspectives of all talented employees worldwide and providing them with the opportunity to power smarter healthcare for everyone, everywhere. When our talented employees bring their authentic selves and their diverse experiences to work, they enable us to accomplish extraordinary things. Multifaceted thought processes spark innovation. Multi-talented collaboration harnesses innovation to deliver superior outcomes. Likewise, as part of this culture, IQVIA is committed to ensuring effective equality between women and men, integrating it as a strategic principle in its corporate and human resources policies.