Job Overview
Serve as a therapeutic and/or operational expert throughout the new business and program/project delivery lifecycle.

Responsibilities

• Lead real-world evidence (RWE) study strategy development

• Partner with Sales, Medical, and Operations teams to develop competitive and operationally feasible solutions for client opportunities.

• Provide expertise in protocol assessment, feasibility strategy, site and country selection, patient recruitment, and study execution planning.

• Support proposal development, bid defense meetings, and client presentations.

• Ensure effective transition of study strategy to project delivery teams and provide strategic guidance throughout study execution.

Qualifications

• Bachelor's degree or above in Life Sciences, Pharmacy, Medicine, Public Health, or a related field.

• 5+ years of experience in clinical research, clinical operations, real-world evidence (RWE), feasibility, or drug development.

• Experience in at least one of the following areas: Clinical Project Management/Real World Evidence/ Feasibility / Protocol Development /Study Strategy

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.