As a Senior Clinical Research Associate at PSI you will enjoy a variety of monitoring tasks and work on clinical studies in different therapeutic indications, maintaining the highest quality standards in the industry and delivering exemplary customer service.
Hybrid role in Ankara, Türkiye
You will:
- 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
- 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
