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 sponsors
• Serves as the primary point of contact for investigative sites and/or sponsors
• Ensures tracking completion of all regulatory and contractual documents for sites

Qualifications

• Bachelor’s Degree in Scientific discipline or Healthcare
• 3 to 5 years prior relevant experience
• Good negotiating and communication skills with ability to challenge.
• Thorough understanding of regulated clinical trial environment and knowledge of drug development process
• Goal 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