Senior Clinical Research Associate

Summary

Join PSI as a Senior Clinical Research Associate and enjoy a variety of monitoring tasks while maintaining the highest quality standards in the industry.

Requirements

• College/University degree in Life Sciences or an equivalent combination of education, training & experience
• Independent on-site monitoring experience in Türkiye
• Experience in all types of monitoring visits in Phase II and/or III
• Full working proficiency in Turkish and English
• Proficiency in MS Office applications
• Ability to plan, multitask and work in a dynamic team environment
• Communication, collaboration and problem-solving skills
• Ability to travel
• Valid driver’s license

Responsibilities

• Conduct and report all types of onsite monitoring visits as well as remote visits
• Perform CRF review, source document verification and query resolution
• Be responsible for site communication and management
• Be involved in site identification process
• Be a point of contact for in-house support services and vendors
• Communicate with internal project teams regarding study progress
• Support regulatory team in preparing documents for study submissions