This Global medical devices company known for developing and delivering effective treatments is located in Sydney and in search of a passionate Clinical Research Associate to jump in and help the team in a very busy period of time. Responsible for any aspects of the clinical trial process you will be required to work closely with the team and on tasks that are required to ensure project timelines and deliverables. There will be monitoring involve and interstate travel of up to 70%. This is a 6-12 month contract starting immediately.
Reporting to the Clinical Operations Manager, your main responsibilities will be general on-site monitoring, verifying that informed consent procedures and protocol requirements are adhered to, ensuring the integrity of the data submitted on CRFs, preparing accurate and timely trip reports as well as being responsible for all aspects of registry management.
To be considered for the role, you will have a Bachelor’s level degree in life sciences or similar discipline, a minimum of 2 years proven experience in independent multi-site clinical monitoring as well as an understanding of clinical trial processes and regulatory requirements. You shall need to be a good planner, organised, have problem solving abilities with strong computer and management skills. If you are a team player and have the ability to work in any area of the process then don’t miss this opportunity to join a dynamic environment alongside a dedicated and passionate team.
For Further information please contact Victoria Andrews on 0282269670 or email your CV to [email protected]
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