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.
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.
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)
Clinical Researches
undefinedPMP® Certification Training Course (36 PDU) (ISTANBUL INSTITUTE)
PMP® Certification Training Course (36 PDU) (ISTANBUL INSTITUTE)
Klinik Araştırmalar Saha Görevlisi (Koordinatörlüğü) kursu (Turkish Clinical Research Association)
Temel İyi Klinik Uygulamalar Kursu (GCP) (Turkish Clinical Research Association)
KOSGEB APPLIED ENTREPRENEURSHIP EDUCATION CERTIFICATE (BIGG-Tübitak - Young Entrepreneurs training camp)