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.
Join us on our exciting journey!
IQVIA™ is The Human Data Science Company™, focused on using data and science to help healthcare clients find better solutions for their patients. Formed through the merger of IMS Health and Quintiles, IQVIA offers a broad range of solutions that harness advances in healthcare information, technology, analytics and human ingenuity to drive healthcare forward.
PURPOSE
Engage in company training program to gain knowledge and skills required to independently conduct clinical remote monitoring visits and other clinical research activities in accordance with study protocol, standard operating procedures, good clinical practice, and applicable regulatory requirements. Gain an understanding of all aspects of Real World Late Phase Research (RWLPR) site management and monitoring by striving to understand the work based on a combination of structured training programs, self-directed use of training materials and experience from study assignments.
RESPONSIBILITIES
The Associate Site Manager is responsible for developing relationship with their assigned clinical trial sites to ensure sites have the information, tools and materials they need to meet the objectives of the study. He/she helps remove roadblocks, answer questions and resolve issues to minimize the burden of study execution on their assigned sites, so site personnel can focus on enrolling patients and capturing data as required by the study.
The Associate Site Manager is responsible for maintaining regular contact with their assigned sites in accordance with the site monitoring agreement for each study. They collect, compile, document and report site related data. They ensure investigative sites are working in accordance with protocol, standard operating procedures, good clinical practice, and all applicable regulatory requirements. They may be responsible for sites participating in one or more studies, and assignments may include site selection, site initiation and enrollment, follow up and site close out.
We know that meaningful results require not only the right approach but also the right people. Regardless of your role, we invite you to reimagine healthcare with us. You will have the opportunity to play an important part in helping our clients drive healthcare forward and
Whatever your career goals, we are here to ensure you get there!
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.