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: - Christine Bristol, Executive Consultant on 02 8877 8766 or at cbristol@hpgconnect.com for a confidential discussion. or Jill Manson, Recruitment Consultant on 02 8877 8733 or at jmanson@hpgconnect.com for a confidential discussion.
