Clinical Research Associate

Benefits

Excellent training and development opportunities

Large CRO working with various Sponsors

Multiple opportunities for various levels of CRAs

Attractive salary package plus other benefits

About the company

Working for a Global CRO with a strong focus and dedication to advancing healthcare in more ways than one. Supporting their clients in pushing the boundaries of science and development to create a healthier world. This company's reach being so large that they work with both core team and FSP models to facilitate growth, research and development in human sciences. This enables delivery of the most recent and best available medication to the public to create a healthier world.

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
• Contribute to the identification of new sites for clinical trials
• Facilitate communication between the internal and external stakeholders and sites
• Facilitate preparation, collection, and oversight of all site documents to ensure trail achieving SOP guidelines
• Monitoring sites and completing reports timely in line with relevant SOP
• Provides protocol and related study training to assigned sites
• Manages site performance and collaborates to complete regulatory submissions & recruitment plans
• Guide investigator re-numeration and financial contracts between the client, sites and investigators

Skills & Experience

• Bachelor's Degree in Life Sciences or other scientific/nursing disciplines is essential
• Must have local independent monitoring experience within a CRA or Pharma company
• Excellent knowledge of international guidelines ICH/GCP, basic knowledge of GMP/GDP
• Preferred experience in monitoring Oncology studies
• Reasonable understanding of Clinical Study Management including monitoring, study drug handling and data management
• Australian working rights
• Ability to travel on a regular basis which will involve interstate travel across ANZ
• Oncology experience is highly desired

How to Apply

Click apply or contact Christine Bristol, Executive Consultant on 02 8877 8766 or at cbristol@hpgconnect.com for a confidential discussion.