Global Feasibility Specialist - Spain

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.