IQVIA™ is the leading human data science company focused on helping healthcare clients find unparalleled insights and better solutions for patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness the power of healthcare data, domain expertise, transformative technology, and advanced analytics to drive healthcare forward.
As a Clinical Trials Regulatory Specialist you will coordinate clinical trials regulatory maintenance process on assigned studies and contact related teams to ensure that process goes smoothly and within expected timelines.
Personally you have advanced level of English, able to maintain effective cross-cultural communication and influence others in order to get things done.
Your main responsibilities as a Clinical Trials Regulatory Specialist will be:
Skills and experience important for the role:
of other combination of skills and experience that will ensure your success at that role.
Join Us
Making a positive impact on human health takes insight, curiosity, and intellectual courage. It takes brave minds, pushing the boundaries to transform healthcare. Regardless of your role, you will have the opportunity to play an important part in helping our clients drive healthcare forward and ultimately improve outcomes for patients.
Forge a career with greater purpose, make an impact, and never stop learning.