Clinical Research Associate – Client-dedicated

• Provide end-to-end clinical trial support from study start-up through monitoring to study close-out
• Perform and coordinate all aspects of the clinical monitoring process
• Conduct monitoring activities independently
• Work in multinational project teams across multiple projects
• Deliver exemplary customer service
• Take ownership of assigned work and contribute to high-quality, cost-efficient clinical studies

• University degree in a life-sciences field
• Experience with independent, on-site monitoring in a pharmaceutical company or clinical research organisation
• Qualified to conduct clinical monitoring activities independently
• Demonstrated understanding of ICH-GCP, EU and FDA requirements
• Demonstrated understanding of medical/therapeutic area knowledge and medical terminology
• Exceptional communication, collaboration, organisational and time management skills
• Fluency in Turkish and English

• Award-winning training programmes to develop technical and professional skills and knowledge
• Remote work arrangement