Regulatory Affairs Professional Opportunity

7 days ago


Melbourne, Victoria, Australia IQVIA Argentina Full time

The Regulatory Affairs Professional Opportunity at IQVIA Australia offers a unique chance to drive clinical research excellence and contribute to groundbreaking advancements in healthcare. As a Senior Clinical Research Associate, you will be responsible for ensuring that our studies are conducted in accordance with regulatory requirements and industry best practices.

We are seeking a highly experienced and skilled professional with a minimum of 4 years of on-site monitoring experience in Australia. Your expertise in Cardiology trial management is an asset, but not essential. What matters most is your ability to communicate effectively, build strong relationships with colleagues, managers, and clients, and demonstrate proficiency in Microsoft Office and relevant technology.

IQVIA is a leading global provider of clinical research services and commercial insights. As a member of our team, you will have access to world-class training and mentoring opportunities, allowing you to grow and develop your skills in a supportive environment.

Responsibilities and Requirements:
  • Study Conduct: Ensure that studies are conducted in accordance with regulatory requirements and industry best practices.
  • Quality Assurance: Identify and mitigate potential quality risks to ensure study integrity.
  • Collaboration and Communication: Build strong relationships with colleagues, managers, and clients to achieve study objectives.


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