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.

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

• 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