Responsible for overseeing clinical trial budgets and leading negotiation activities on a global scale

Essential Functions

Preparation, review, negotiation and management of site regulatory documentation and clinical trial agreements with sites and sponsorsMaintains, reviews, and reports on site activation performance metricsServes as the primary point of contact for investigative sites and/or sponsors;Ensures tracking completion of all regulatory and contractual documents for sitesEstablishes project timelines.Ensures all site activation activities are performed in accordance with all regulations, SOPs, Work Instructions and project requirements either at the global, regional, or country level and all relevant documents are submitted timely to the Trial Master File as per IQVIA/Sponsor requirements.Establishes and/or executes goals and objectives for team(s) as well as tracking and delivering on operational/financial performance.Participates in the broader Global Site Activation planning process; contributes to long-mid range goals and plans; and coordinates activities with other managers and their respective sub-families. 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 materialsPreparation, 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

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.