When our values align, there's no limit to what we can achieve.
At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.
This Senior Regulatory Affairs Associate is for FSP team to provide post-authorization lifecycle management, prepare/ organize/ coordinate local specific documentation to maintain regulatory compliance and support HA inspections, as needed.
Strong knowledge and hands-on experience in Australia and New Zealand is required.
Key Accountabilities:
Project Execution
Consulting Activities and Relationship Management
Business Development
Parexel-Related Activities
Skills:
Knowledge and Experience:
Education:
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