Summary
Overview
Work History
Education
Skills
Certification
Timeline
Generic

Müge Etik

Site/Study Coordinator In Clinical Researches
Maltepe

Summary

Highly interested with over 2 years of experience in a multidisciplinary Clinical Research as a Site Coordinator. My goal is to secure a role as a Clinical Research Associate (CRA), leveraging my experience in both Clinical Research and R&D within the pharmaceutical industry. Holding a Master of Science (M.Sc) degree with a focus on Molecular Biology from the Graduate School of Natural and Applied Sciences, Eager to contribute my skills and knowledge to further advancements in healthcare. Thank you for considering my application.

Overview

5
5
years of professional experience
8
8
years of post-secondary education
4
4
Certifications
2
2
Languages

Work History

Site/Study Coordinator in Clinical Researches

Innovex A.Ş.
02.2022 - 03.2024

Diligently collected and managed data in accordance with research protocols and operational guidelines.
Collected Informed Volunteer Consent Forms from 60 patients with specific genetic mutations for research studies.
Proficient in collecting, evaluating, and processing study data using Excel and REDCap software.
Coordinated patient visits and ensured compliance with research protocols.
Proactively addressed study-related issues and facilitated interdisciplinary meetings with 21 different departments.
Known for improving processes, adhering to procedures, and supporting team goals.
Possess strong reliability, organizational skills, and the ability to manage multiple priorities effectively.

R&D Personnel

Vision Biotechnology
04.2021 - 06.2021

Real Time PCR kit production and optimization
Real Time PCR analysis
One-Step RT-qPCR
Master mix preparation
Production of DNA and RNA isolation kits
Food safety studies (medium preparation, bacterial cultivation, DNA isolation from isolated bacteria species and two-step RT-qPCR analysis)

R&D Documentation

Genveon İlaç
08.2019 - 01.2021
  • Project follow-up and Reporting: To follow up the processes of Tübitak TEYDEB projects, to prepare the documentation and report presentations of the interim technical reports, to ensure communication with the lecturers who follow the project, and to answer the questions from the Tübitak institution by preparing the necessary technical documents.
  • Licensing: To prepare the sections of the CTD (common technical documents) files concerning R&D (Module 3) for the Ministry of Health application.
  • To write SOP (standard operation procedures).

Education

Master of Science - Graduate School of Natural And Applied Sciences

Muğla Sıtkı Koçman University
Muğla, Turkey
02.2014 - 08.2017

Bachelor of Science - Biology

Muğla Sıtkı Koçman University
Muğla, Turkey
09.2008 - 08.2013

Skills

Clinical Researches

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Certification

PMP® Certification Training Course (36 PDU) (ISTANBUL INSTITUTE)

Timeline

PMP® Certification Training Course (36 PDU) (ISTANBUL INSTITUTE)

03-2022

Site/Study Coordinator in Clinical Researches

Innovex A.Ş.
02.2022 - 03.2024

Klinik Araştırmalar Saha Görevlisi (Koordinatörlüğü) kursu (Turkish Clinical Research Association)

02-2022

Temel İyi Klinik Uygulamalar Kursu (GCP) (Turkish Clinical Research Association)

02-2022

R&D Personnel

Vision Biotechnology
04.2021 - 06.2021

R&D Documentation

Genveon İlaç
08.2019 - 01.2021

KOSGEB APPLIED ENTREPRENEURSHIP EDUCATION CERTIFICATE (BIGG-Tübitak - Young Entrepreneurs training camp)

10-2018

Master of Science - Graduate School of Natural And Applied Sciences

Muğla Sıtkı Koçman University
02.2014 - 08.2017

Bachelor of Science - Biology

Muğla Sıtkı Koçman University
09.2008 - 08.2013
Müge EtikSite/Study Coordinator In Clinical Researches