Job details

Location
New South Wales
Salary
AU$52000 - AU$110000 per annum + Attractive Benefits!
Job Type
Full Time
Ref
BBBH35191_1598594724
Contact
Chanelle Wilson
Contact email
Email Chanelle
Contact phone
+61288778772
Posted
24 days ago

Job details

Location
New South Wales
Salary
AU$52000 - AU$110000 per annum + Attractive Benefits!
Job Type
Full Time
Ref
BBBH35191_1598594724
Contact
Chanelle Wilson
Contact email
Email Chanelle
Contact phone
+61288778772
Posted
24 days ago

Benefits

  • Excellent training and development opportunities
  • Large CRO working with various Sponsors
  • Large focus on Oncology and Autoimmune disease research
  • Attractive salary package plus car allowance
  • Flexible Working arrangements - Home / Office based


About the company

  • Working for a Global full service CRO on global delivery, scientific leadership, and various therapeutic specialities to deliver and create world-class solutions in healthcare. With a strong focus on quality and efficient delivery of every phase of research clinical trials. Supporting various clients across pharmaceuticals, medical devices and diagnostic research and development through all trial phases as well as registration and post-marketing trials.


About the opportunity

  • The CRA 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.


Responsibilities

  • Ensures time-lines are met from start up to closeout
  • 30-60% non-local, national travel
  • 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

  • Must have Australian independent monitoring experience of at least 2 years
  • Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP
  • Preferred experience in monitoring Oncology or Autoimmune disease studies
  • Reasonable understanding of Clinical Study Management including monitoring, study drug handling and data management
  • Australian working rights


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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