Regulatory Affairs Consultant - Core Team

Parexel · Australia

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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.

Knowledge in Regulatory Affairs Activities, focusing on CTAs (Phase I-IV) for various Therapeutic Areas

Proficient in Regulations, ideally with some knowledge in New Zealand

Preferred experience: Phase I or Early Phase studies, Studies involving Medical Devices, GMOs, Radiopharmaceuticals, Biological Drugs, Labelling for Investigational Medicinal Products

Experience in Quality Documentation and CMC (Composition, Manufacturing and Control of Investigational Medicinal Products) could be a plus.

Key Accountabilities:

Project Execution

Consulting Activities and Relationship Management

Business Development

Parexel-related Activities

Skills:

Knowledge and Experience:

Education:

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