IQVIA Real World Late Phase CRA - office or home based in Belgium in Vilvoorde, Belgium
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.
As you develop your career as a CRA, this role is an ideal stepping-stone. It offers you a unique opportunity to expand your skills and experience in the realm of real-world and late phase research. You will also have training and development to plan and progress your career in the direction you choose. And you will not do it alone – you will have dedicated mentoring and receive structured quarterly reviews to enable your performance and success.Award winning and innovative, we’ll give you access to cutting-edge in-house technology, allowing you to work on global projects but with a mostly regional / home state travel remit. You’ll be building a smart and flexible career with no limits. While projects vary, your typical responsibilities might include:
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Supporting the development of a subject recruitment plan
Establishing regular lines of communication plus administering protocol and related study training to assigned sites
Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements. You should have:
A Bachelor's degree or higher level degree in a health care or other scientific discipline or educational equivalent
Preferrably 1-3 years of on-site monitoring experience
Alternatively, you should have an equivalent combination of education, training and experience
Oncology experience would be appreciated
Fluent written and verbal communication skills in Dutch and French including good command of English language
You will need to be comfortable collaborating and communicating with a variety of colleagues and customers and with travelling of up to 40%
Ideally, you will also have a good knowledge of applicable clinical research regulatory requirements
If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team . Connect to great opportunity™
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 ultimately improve human health outcomes. Whatever your career goals, we are here to ensure you get there! We invite you to join IQVIA™
At IQVIA, we have a vision. Where every healthcare decision is based on evidence. Where data science and human science come together to improve global health. Where new and creative solutions aren’t just possible – they are expected.
Thank you for your interest in growing your career with us. It takes insight, curiosity, and intellectual courage to transform healthcare. The 56,000+ employees of the IQVIA family of companies, including Q2 Solutions, are reimagining a world without the consequences of disease. We are brave minds bringing powerful ideas to reality. At IQVIA, you can truly make an impact in an environment where you’re supported to succeed.
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