Fulya Taylan

Background

About Fulya Taylan

I am a life sciences professional with over 23 years of experience in molecular biology, genetics, and research in rare diseases and childhood cancer predisposition. Throughout my career, I've worked in diverse teams to tackle data-driven projects. My research has led to more than 55 peer-reviewed publications and significant contributions in genomics, rare diseases, and childhood cancer predisposition. I have collaborated with researchers from diverse cultures and backgrounds. As a course leader, I've guided master's-level students in molecular genetics, developing my ability to communicate complex concepts clearly and accessibly. I'm deeply committed to inclusivity, with training in intercultural communication, gender equality, and sustainability. I thrive in interdisciplinary, fast-paced environments where creativity and collaboration drive results. From interpreting genomic data to organizing events and coordinating projects, I excel at turning challenges into actionable solutions. I'm seeking to transition and leverage my research expertise, strategic thinking, and passion for problem-solving on a broader stage. I'm particularly interested in partnering with healthcare and life sciences organizations to improve patient outcomes, optimize processes, and develop innovative strategies. If you'd like to connect or explore how my expertise could add value to your organization, please reach out. I'm open to opportunities across Europe.