Single Sponsor (senior) CRA - home or office based in Belgium (R1055584) in Zaventem, Belgium at IQVIA™

Date Posted: 8/7/2019

Job Snapshot

  • Employee Type:
    Full-Time
  • Experience:
    Not Specified
  • Date Posted:
    8/7/2019
  • Job ID:
    R1055584

Job Description

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.

In our sponsor-dedicated model, you will work in a close partnership with one of our key customers in order to deliver a comprehensive clinical trial management. Within this team, you will focus on different projects of this single biopharma client(s) in Belgium and gain direct and in-depth experience of working with this sponsor.

Home-office solutions, flexible working hours and a company car will offer you flexibility in structuring your working days and will guarantee a good work life balance.

As you develop your career as a CRA or Sr CRA, this role offers you the opportunity to plan and progress your career in the direction you choose. At IQVIA, we do not believe in a ‘career ceiling.’ You can make this role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. And you won’t do it alone – you will have dedicated mentoring and receive structured quarterly reviews on performance, promotion and bonus awards.

While projects vary, your typical responsibilities might include: 

  • Performing site selection, monitoring and close-out visits, plus maintaining appropriate documentation
  • Establishing regular lines of communication plus administering protocol and related study training to assigned sites
  • Supporting the development of a subject recruitment plan
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Leading and managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution 
  • Onsite monitoring (and if needed remote monitoring)
  • Handling safety reporting and submissions to ethic committee

You should have:

  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
  • At least 1.5-2 years of on-site monitoring experience
  • Alternatively, you should have an equivalent combination of education, training and experience 
  • Fluent written and verbal communication skills in Dutch and French, including good command of English
  • You will need to be comfortable collaborating and communicating with a variety of colleagues and customers
  • Ideally, you will also have a good knowledge of applicable clinical research regulatory requirements
  • Willingness to travel within different regions in Belgium

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 teamConnect to great opportunity™

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.



Job ID: R1055584