Job Description & Requirements
Reporting to the Regulatory Affairs Manager, you will be responsible for assisting in Regulatory Affairs activities for clinical trials and marketing authorisation.
Responsibilities
- Assist with submission of applications and variations for clinical trials and marketing authorisation across all pipelines
- Support regulatory assessment of submission requirements based on relevant regulations
- Assist with administrative work necessary to support regulatory activities
- Review and provide input for regulatory documents
- Support any other duties assigned
Qualifications
- Degree in Biological, Chemistry, or a related field
- No experience required. Must have an interest in Regulatory Affairs
- Keen learner with a strong attention to detail and organizational skills
- Proficiency in English (written and spoken) is required
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