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Senior/Clinical Research Associate

Healthcare Professionals Group

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About the opportunity

The CRA/SCRA is responsible for the preparation, initiation, monitoring and closure of an agreed number of centres in clinical studies according to Procedural Documents, international guidelines such as ICH and GCP as well as relevant local regulations. Deliver according to the commitment in the individual trials.


  • Ensures time-lines are met from start up to closeout
  • Monitoring sites and completing reports timely
  • Maintaining clear lines of communication with sites
  • Provides protocol and related study training to assigned sites
  • Manages site performance and collaborates to complete regulatory submissions & recruitment plans

Skills & Experience

  • Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP
  • Minimum of two years independent monitoring experience
  • Good medical knowledge preferably experience in monitoring Oncology studies
  • Good understanding of Clinical Study Management including monitoring, study drug handling and data management

How to Apply

Click apply or contact Chanelle Wilson, Recruitment Consultant on 02 8877 8772 or at cwilson@hpgconnect.com for a confidential discussion.

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