Thomas Eskildsen

Having worked with both major global pharmaceutical companies and small biotech start-ups, Thomas has more than 15 years of experience working with the clinical trials. Thomas’ work has been focused on all aspects of clinical trial managing including budget and timelines management, sponsor oversight, protocol and informed consent development, development study-specific documents, team training, data cleaning, and patient recruitment.

He holds an MSc. in Pharmaceutical Sciences and BSc. in Biotechnology.