
Selda Samakoglu, MD, PhD
Dr. Selda Samakoglu is a distinguished medical oncologist, physician-scientist, and biopharmaceutical executive with over 20 years of experience spanning academia, clinical medicine, and industry.
Most recently, she served as Vice President of Clinical Sciences at Iovance Biotherapeutics, where she led global development of cell-based therapies for hematologic malignancies and solid tumors including non-small cell lung cancer and head and neck cancer. She has also held executive leadership roles at ImClone Systems, Gilead Sciences, Bristol Myers Squibb, CSL Behring, Boehringer Ingelheim, and Replimune. Over her career, she has successfully led programs from IND through proof-of-concept to NDA/BLA approvals across a wide range of modalities, including monoclonal antibodies, small molecules, oncolytic viruses, and cell-based immunotherapies. She played pivotal roles in the regulatory approvals of Cetuximab (colorectal cancer), Imbruvica (marginal zone lymphoma), Elotuzumab (multiple myeloma), and Amtagvi (melanoma).
Dr. Samakoglu has engaged with global health authorities including the FDA, EMA, CDE, and MHRA. Her work has been instrumental in advancing innovative therapies through complex clinical and regulatory pathways.
Dr. Samakoglu earned her BS and MD from Hacettepe University School of Medicine in Turkey, followed by specialization in Pediatric Hematology/Oncology at both Hacettepe and Mount Sinai School of Medicine in New York. She holds a PhD in Medical Biology and Human Genetics from a joint program between Erasmus University School of Medicine in the Netherlands and Akdeniz University. She completed postdoctoral clinical and research fellowships at Institut Pasteur in Paris and Memorial Sloan Kettering Cancer Center in New York.
At Aveta, she leads clinical development of the company’s oncology drugs.