About the Company

Our client is a pioneering medical device company that is currently developing a novel neurostimulation technology to treat Obstructive Sleep Apnoea for patients that have failed or refused continuous positive airway pressure (CPAP) therapy.

About the opportunity

This company are currently seeking a Senior Clinical Research Associate with data management experience to join their clinical research team based in Australia. Working from home, the position requires regular travel to conduct monitoring visits at our clinical trial sites across Australia.

Responsibilities

You will be responsible for conducting the full scope of CRA duties including conducting all clinical monitoring and site management activities. Working in accordance with applicable ICH-GCP guidelines and regulatory requirements.

Skills and Experience

• Bachelor's degree or RN in a related field or equivalent
• Understanding of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
• Min 3 years' independent monitoring experience
• Solid understanding of clinical trial design, trial execution and operations
• Some Knowledge of international standards (FDA, EMEA) and local regulations
• Proven expertise in working in teams collaboratively
• Strong knowledge and experience undertaking monitoring and data management for device studies is strongly preferred.
• Self-motivated, able to work remotely, independently and with a team while managing own schedule
• Travel as necessary according to project needs.
• Skill in managing multiple priorities
• Able to work in an international environment with internal & external team partners (including virtual teams) across time zones

Why this opportunity is right for you

• Fantastic opportunity to work with a fast-growing medical device company
• Strong career progression opportunities
• Work from home

How to Apply

Click apply or contact Maddy Rhodes-Laird, Senior Recruitment Consultant on 03 9938 7101 for a confidential discussion.