Senior Clinical Research Associate or Clinical Research Associate (Client

As a Senior Clinical Research Associate or Clinical Research Associate, you will be responsible for site selection, initiation, monitoring, and close-out visits, as well as supporting subject recruitment and managing progress on global trials. You will need to have a good knowledge of clinical research regulatory requirements and be comfortable collaborating with colleagues and customers.

Requirements

• University degree in scientific discipline or healthcare
• At least 1 year of on-site monitoring experience
• Good knowledge of GCP and clinical research regulatory requirements
• Good computer skills including MS Office
• Excellent command of English language
• Organizational, time management and problem-solving skills
• Ability to establish and maintain effective working relationships with colleagues, managers, and customers.

Benefits

• Attractive remuneration package
• Career development opportunities
• Flexible work schedules/arrangement
• Excellent working environment
• Programs to help build technical skills and therapeutic knowledge