Single Sponsor (senior) CRA - home or office based in Belgium

08 Jan 2019
22 Feb 2019

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 team. Connect to great opportunity™

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