
I am Enes Keskin. I studied Biology at Hacettepe University Faculty of Science. After graduating, I had worked different laboratory areas; flow cytometry, microbiology, biochemistry, hematology, COVID-19 PCR laboratory for 3 years. After that, I had worked as site coordinator at Ankara University Faculty of Medicine at Hematology Department from Aug 2022 to Jan 2024 and then I currently work at Ankara Liv Hospital Department of Oncology.
Medication Dispensing
Military Service: Done
Driver's License: B
Study Phase: Phase II - Phase III
Indication: Diffuse Large B-cell Lymphoma
Role: Clinical Research Coordinator
-Scheduled and coordinating patients' visits
-Organize the site for patient visit
-Check patient eligibility with PI
-Keep inform PI about visit procedures
-Write source document under PI supervision
-Prepare laboratory samples and send them to the central lab
-Enter all data in the e-CRF -Assign study drug and dispense
-Report all adverse and serious adverse events
-Management of queries
-Management of ISF.
Study Phase: Phase II - Phase III
Indication: Chronic Lymphocytic Leukomia
Role: Clinical Research Coordinator
-Scheduled and coordinating patients' visits
-Organize the site for patient visit
-Check patient eligibility with PI
-Keep inform PI about visit procedures
-Write source document under PI supervision
-Prepare laboratory samples and send them to the central lab
-Enter all data in the e-CRF -Assign study drug and dispense
-Report all adverse and serious adverse events
-Management of queries
-Management of ISF.
Study Phase: Phase III
Indication: Melanoma
Role: Clinical Research Coordinator
-Scheduled and coordinating patients' visits
-Organize the site for patient visit
-Check patient eligibility with PI
-Keep inform PI about visit procedures
-Write source document under PI supervision
-Prepare laboratory samples and send them to the central lab
-Enter all data in the e-CRF -Assign study drug and dispense
-Report all adverse and serious adverse events
-Management of queries
-Management of ISF.
Study Phase: Phase III
Indication: Non-Small Cell Lung Cancer
Role: Clinical Research Coordinator
-Scheduled and coordinating patients' visits
-Organize the site for patient visit
-Check patient eligibility with PI
-Keep inform PI about visit procedures
-Write source document under PI supervision
-Prepare laboratory samples and send them to the central lab
-Enter all data in the e-CRF -Assign study drug and dispense
-Report all adverse and serious adverse events
-Management of queries
-Management of ISF.