(Senior) Clinical Research Associate

This role can only be considered  in Adelaide or Perth 

Are you a Clinical Research Associate or Senior Clinical Research Associate looking for a new and exciting challenge with opportunity for ongoing support and growth? Are you looking for a career and not just a job? Then we have the role for you!

Key Responsibilities

• Perform site selection, initiation, monitoring and close-out visits and work with sites to adapt, drive and track subject recruitment plans
• Provide monitoring visits and site management for a variety of protocols, sites and therapeutic areas
• Administer protocol and related study training to assigned sites and establish regular lines of communication
• Evaluate the quality and integrity of study site practices related to the proper conduct of the protocol and adherence to applicable regulations
• Manage the progress of assigned studies by tracking regulatory submissions and approvals, recruitment and enrolment, case report form (CRF) completion and submission, and data query generation and resolution.
• Create and maintain appropriate documentation regarding site management, monitoring visit findings and action plans
• Collaborate and liaise with study team members for project execution support as appropriate.

Not everyone can be a CRA it’s an extraordinary role, do you meet this unique criteria?

• Bachelor's degree in Life Sciences or other scientific/nursing disciplines is essential
• Minimum of 2 years independent site monitoring experience
• CRO experience is highly desired
• Ability to travel on a regular basis which will involve interstate travel
• Extensive knowledge of Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines is required