About the company

This global CRO are committed to developing groundbreaking devices and new pharmaceutical products.

About the opportunity

In this role, you will responsible for ensuring the timely submission of regulatory documents related to clinical trial activity

Duties

• Perform required activities within the country that lead to activation of investigative sites in all phases of clinical trials
• Prepare, review, and submit to regulatory agencies (TGA / Medsafe
• Provide expertise and guidance to global study teams in regard to regulatory activities
• Track regulatory submissions

Skills and Experience

• Scientific qualifications
• Minimum of 2 years' experience in a similar role
• Experience in preparing and submitting TGA regulatory applications
• Excellent organisation and communication skills

• Proactive approach
• Demonstrated willingness to learn

Benefits

• Great offices
• Established, friendly team

How to Apply

Click apply or contact Jo Turner, Senior Specialist Manager on 03 9938 71020 for a confidential discussion.

About us

Healthcare Professionals Group. Recruiting all positions, at all levels, into biotechnology, medical devices, pharmaceutical and scientific companies. For more pharmaceutical, medical or healthcare related job opportunities visit www.hpgconnect.com

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