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CRA/ SrCRA, GFR Roche. Johannesburg. Role will be homebased - (1805110) in Pretoria, ZA at IQVIA™

Date Posted: 4/2/2018

Job Snapshot

Job Description


Whether you’re beginning or continuing your career as a CRA, this role is an ideal stepping-stone. You’ll have training and development to plan and progress your career in the direction you choose. 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’ll 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’ll 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 
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.

Job Requirements

You should have:
  • A Bachelor's degree in a health care or other scientific discipline or educational equivalent
  • Successful completion of a CRA Trainee Program or at least three months of on-site monitoring experience
  • Alternatively, you should have an equivalent combination of education, training and experience 
 

Job ID: 1805110