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Job Details

*RWLP CRA or Associate CRA (f/m) - office-based in Basel or home-based throughout Switzerland*

Company: Quintiles
Location: Basel
Reference: 1802555
Closing Date: 29 Apr 18
Type: Full Time
Salary (£): Negotiable
Benefits:

Job Summary:

As you develop your career as a  (associate) CRA or Senior 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 the Associate CRA/Senior CRA role a stepping-stone into wider opportunities like operations management, dedicated customer solutions, and project management. ...

Requirements:

As you develop your career as a  (associate) CRA or Senior 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 the Associate CRA/Senior CRA 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.
 
Award winning and innovative, we will give you access to cutting-edge in-house technology, allowing you to work on global projects but with a regional / home state travel remit, so no need for national travel in certain countries. You will 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
  • Performing site identification activities
  • Performing submission activities
 
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 in a health care or other scientific discipline or educational equivalent
  • At least one year of on-site monitoring experience (preferrably)
  • Alternatively, you should have an equivalent combination of education, training and experience
  • Excellent communication skills in English language including fluent language skills in Italian and in French are a required
 
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
 
 

Apply for this job: *RWLP CRA or Associate CRA (f/m) - office-based in Basel or home-based throughout Switzerland*

Contact Information:

Address:  .
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England
Website:  Visit Our Web Site

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