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