Benefits

• Excellent training and development opportunities
• Attractive salary package plus car allowance
• Flexible Working arrangements - Home / Office based
• Single Sponsor

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 New Zealand independent monitoring experience of at least 6 months
• 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
• NZ working rights

How to Apply

Click apply or contact: Mattias Fitzgerald. Phone: +61 2 8877 8749. Email: MFitzgerald@hpgconnect.com