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 7103 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
