Summary
Overview
Work History
Education
Skills
Additional Information
Clinical Trial Experience
Timeline
Generic

Enes Keskin

Clinical Research Coordinator
Ankara

Summary

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.

Overview

2
2
years of professional experience

Work History

Clinical Research Coordinator

MEDEX SMO
10.2023 - Current
  • Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
  • Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
  • Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines.
  • Provides medical care to patients, always ensuring patient safety comes first.
  • Maintained compliance with regulatory guidelines through rigorous documentation and protocol adherence.

Clinical Research Coordinator

MediSMART CRO
08.2022 - 10.2023


  • Facilitated clear communication between principal investigators, sponsors, and study participants for seamless trial execution.
  • Schedules subject visits within protocol windows, ensuring scheduling capacity is maximized.
  • Enhanced patient safety by meticulously monitoring and documenting adverse events during clinical trials.
  • Conducts clinical studies according to FDA/GCP and ICH regulations and guidelines.
  • Provides medical care to patients, always ensuring patient safety comes first.

Education

Bachelor of Science -

Hacettepe University
Ankara, Turkey
04.2001 -

Skills

Medication Dispensing

Additional Information

Military Service: Done


Driver's License: B

Clinical Trial Experience

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.

Timeline

Clinical Research Coordinator

MEDEX SMO
10.2023 - Current

Clinical Research Coordinator

MediSMART CRO
08.2022 - 10.2023

Bachelor of Science -

Hacettepe University
04.2001 -
Enes KeskinClinical Research Coordinator