Ilayda Ozturk

Goztepe Prof. Dr. Suleyman Yalcin City Hospital – Oncology Department

Working under the supervision of Prof. Dr. Mahmut Gumus for clinical trials sponsored by MSD.

Key responsibilities include:

• Supporting Principal and Sub-Investigators in subject recruitment and informed consent process
• Source documentation and protocol compliance tracking
• Scheduling and coordinating patient visits, assessments, and follow-ups per protocol timelines
• Timely entry and updating of eCRFs and query resolution
• Reporting adverse events (AEs) and serious adverse events (SAEs) via appropriate systems
• Maintaining and reconciling investigational product (IP) and trial master files (ITFs/eTMFs)
• Managing lab kit orders and sample shipments in alignment with study procedures
• Additionally:
• Collaborate closely with sponsor CRAs during monitoring visits and audits
• Ensure all activities are performed in compliance with ICH-GCP guidelines and local regulations
• Experience in managing multiple protocols simultaneously, prioritizing tasks, and problem-solving under pressure

• Capabilities: DNA/RNA Isolation, Conjugation preparation, Cell Culture, Bacterial cultivation, Measurement of DNA concentration and purity, Media preparation, Clinical research, Real-time qPCR, RT-qPCR, Test kit preparation
• Conducted literature reviews to support ongoing biotechnology research projects.
• Assisted in the development and optimization of laboratory protocols.
• Collaborated with team members to maintain accurate documentation of experimental results.

• I completed my volunteer internship by working actively in the production and quality control department at Bork Health pharmaceutical company.