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Job Details

Clinical Research Associate (sponsor dedicated - home or office based)

Company: Quintiles
Location: Halle-Vilvoorde
Reference: 1801014
Closing Date: 01 May 18
Type: Full Time
Salary (£): Negotiable
Benefits:

Job Summary:

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. ...

Requirements:

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
  • Evaluating the quality and integrity of site practices – escalating quality issues as appropriate
  • Leading progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution 
  • Onsite and 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 two 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 language
  • 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
  • Preferrably experience within medical devices and cardiology
  • Willingness to travel to Netherlands and 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™

Apply for this job: Clinical Research Associate (sponsor dedicated - home or office based)

Contact Information:

Address:  .
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England
Website:  Visit Our Web Site

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