Essential Functions

Responsible for the development of complex contracting strategies, coordination of investigator grants, as applicable and proposal text to support the proposal development process.Develop contract and budget templates and contracting systems, tools, processes, and training materials Preparation, review, negotiation and management of site regulatory documentation and clinical trial agreements with sites and sponsorsServes as the primary point of contact for investigative sites and/or sponsorsEnsures tracking completion of all regulatory and contractual documents for sites

Qualifications

Bachelor’s Degree in Scientific discipline or Healthcare3 to 5 years prior relevant experienceGood negotiating and communication skills with ability to challenge.Thorough understanding of regulated clinical trial environment and knowledge of drug development processGoal oriented, self-starter with proven ability to work independently.

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