Regulatory Affairs Associate

About the company

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

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About the opportunity

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

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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

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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

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Benefits

• Great offices

• Established, friendly team

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How to Apply

Click apply or contact Jo Turner, Senior Specialist Manager on 03 9938 7103 for a confidential discussion.

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About us

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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

( SK915725A )

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