Job Summary

• You will participate in the management of clinical trials by supporting the Clinical Study Manager and coordinating clinical trial teams to ensure successful execution of activities.
• The role includes drafting and reviewing clinical trial documents, ensuring regulatory compliance, overseeing CRO activities, and managing the Trial Master File to maintain inspection readiness.
• The company offers an attractive remuneration and benefits package including incentives, profit-sharing, employee shareholding, health insurance, holidays, and public transport participation.

Matching Summary

Salary

Base: Not specified; Bonus/Equity: Incentives and profit-sharing; Benefits: Health and provident insurance, employee shareholding, holidays, public transport participation

Skills & Requirements

Key Requirements

• Bachelor’s degree or equivalent
• Specialized training as Clinical Research Associate or health-related field
• At least 5 years’ experience in clinical research
• Fluency in spoken and written English

Work Rights