Clinical Research Associate (I-III) - Remote

Overview

This is an incredible CRA opportunity allowing all CRAs to monitor an average of 6 visits per month, allowing YOU to decide what sites can be monitored remotely and which will need an in-person visit.

In Short

• Monitor an average of 6 visits per month.
• Decide which sites can be monitored remotely.
• Excellent work-life balance with minimal red tape.
• Flat hierarchy and great flexibility in work.
• Work on a maximum of 3 protocols.
• Option to work with multi-sponsors or on FSP model.
• Low staff turnover rate in the Turkey CRA team.
• Focus on quality over quantity in monitoring visits.
• Participate and act as Lead CRA on studies.
• Maintain tracking records for assigned sites.

Requirements

• Independent on-site monitoring experience.
• Experience in all types of monitoring visits in Phase I and/or II preferred.
• Oncology and Rare Disease experience highly desirable.
• Proficiency in MS Office applications.
• Ability to plan, multitask, and work in a dynamic team environment.
• Ability to travel.

Benefits

• Flexible working conditions.
• Opportunity to work with multiple sponsors.
• Supportive team environment.
• Focus on quality monitoring.
• Low staff turnover.