Clinical Trial Associate

• Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements
• Maintain and organize clinical trial documentation, including study files, essential documents, and regulatory submissions
• Support the preparation of study-related materials, such as informed consent forms and case report forms
• Work with cross-functional teams to facilitate communication and ensure smooth trial execution
• Contribute to the tracking and reporting of clinical trial metrics and milestones

• Bachelor's degree in a scientific or healthcare-related field
• Prior experience or strong interest in clinical research
• Knowledge of clinical trial processes, regulations, and guidelines
• Excellent organizational and communication skills
• Ability to work collaboratively in a fast-paced environment with attention to detail
• Willingness to travel as required (approximately 10%)
• Legal right to work in the country where the role is based

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways