Senior Regulatory Affairs Associate – Regulatory Affairs Generalist
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Job Description
Senior Regulatory Affairs Associate ensuring compliance and documentation for clinical trials at Parexel. Collaborating with local and global teams to maintain regulatory standards and client expectations.
Responsibilities:
- Support Global and/or local Regulatory teams
- Prepare and coordinate documentation to meet national submission requirements
- Maintain regulatory compliance and support HA inspections
- Serve as main client contact and ensure project quality and timeliness
Requirements:
- 3-5 years of experience in an industry-related environment in Australia including New Zealand
- Excellent interpersonal and intercultural communication skills, both written and verbal
- Knowledge of regulatory requirements and guidelines
- Bachelor’s Degree in a Scientific or Technical Discipline
Benefits:
- Health insurance
- Retirement plans
- Paid time off
- Flexible work arrangements
- Professional development
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