Essential Functions
- Preparation, review, negotiation and management of 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 contractual documents for sites
- Establishes project timelines.
- Establishes and/or executes goals and objectives for team(s) as well as tracking and delivering on operational/financial performance.
- 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
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
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.
