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 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™

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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.