Ka Yan Chung

Highly skilled R&D scientist/leader with 4 years of experience in clinical studies and project management. Effective communicator. Independent team player known for successfully managing multiple priorities within tight timelines.

As the Head of Clinical Affairs at Credo Diagnostics Biomedical, I oversee all clinical studies and lead clinical operations to support FDA and/or EU-notified body approval for innovative diagnostic products. I have a PMP certification and more than five years of experience in clinical development and project management in the biotechnology industry.

I have a strong background in cellular and molecular biology, with a PhD in Biological Sciences and a track record of leading multi-omic, multi-cancer biomarker discovery projects. I have developed and validated microRNA diagnostic kits, optimized exosome RNA extraction methods, and led high-throughput miRNA profiling. I am passionate about advancing personalized medicine and improving patient outcomes through cutting-edge diagnostics.

I am also a team player, a good communicator, and a detail-oriented and analytical thinker.

I have a PhD with a thesis on dengue virus.