Zeynep Çeker

• Followed clinical research protocols and conducted study visits in compliance with ICH/GCP and FDA regulations.
• Assessed patients'' eligibility criteria following strict adherence to inclusion/exclusion guidelines.
• Trained new team members on essential clinical research protocols and procedures, promoting a culture of continuous learning.
• Worked with principal investigator and sponsors to facilitate daily trial activities and comply with research protocols.
• Successfully completed 2 audit visits
• Improved data integrity and accuracy with meticulous oversight of data collection processes.
• Facilitated communication between research team and study sponsors, ensuring clear and consistent updates on trial progress.
• Managed study budget effectively, minimizing unnecessary expenses and allocating funds wisely.
• Streamlined data collection processes for increased efficiency and accuracy in study results.

Creating the first database in Türkiye where pollen and images are shared

• Supported staff members in their daily tasks, reducing workload burden and allowing for increased focus on higher-priority assignments.
• DNA and protein purification processes were carefully monitored and implemented.
• Collecting DNA samples from individuals