IQVIA

*RWLPR Associate CRA, CRA or Senior CRA (f/m) - office-based or home-based in Austria*

Company
IQVIA
Location
Austria
Salary
Competitive
Posted
08 Jan 2019
Closes
22 Feb 2019
Ref
R1058967

We are offering an exciting job opportunity as Associate CRA, CRA or Senior CRA (f/m) to work mainly in the field of Late Phase / Non-Interventional Studies and to join our RWE Department office-based or home-based in Austria.  

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 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 for Phase IV/NIS projects
  • 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
  • Taking part in the study start-up process - contracts management, EC, CA submissions 
  • Covering Austria, it might be that covering sites in Germany and Switzerland is occasionally included

You should have: 

  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
  • At least three years of on-site monitoring experience
  • Alternatively, you should have an equivalent combination of education, training and experience 
  • Fluent German and English language skills
  • 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.

Monthly gross salary: starting at 2.000 EUR basic - an overpay is possible according to skills and working experience.

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. 

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