Job Summary

The Global Site Identification and 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.

• Analytical thinker with great attention to detail.

• Good knowledge of concepts of clinical research and drug development.

• Experience collaborating with internal and external stakeholders.

• Ability to prioritize multiple projects and tasks within tight timelines.

• Excellent written and verbal communication skills.

•Demonstrated administrative and project management abilities in an academic, CRO or sponsor environment.

•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