Job Overview
Supports the preparation of regulatory documents and submissions.  May provide support to department staff.  May coordinate specific regulatory tasks, under guidance of senior staff.

Essential Functions
• Sr Reg Doc Coord

Qualifications
• High School Diploma or equivalent Supports the preparation of regulatory documents and submissions. May provide support to department staff. May coordinate specific regulatory tasks, under guidance of senior staff. Req
•  High School diploma
• Science degree preferred, ie biology or microbiology, or biotechnology, pharmacy.
• Good interpersonal communication and organization skills
• Superior word processing skills and detailed knowledge of core software packages, including MS Office applications
• Good attention to detail and accuracy
• General awareness and knowledge of applicable regulatory requirements
• Ability to work on more than 1 project with direction from senior staff as appropriate
• Ability to follow SOPs
• Ability to establish and maintain good working relationships with co-workers, managers and clients

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.