Daniel Wood is a seasoned professional with over 20 years of clinical development experience, including more than 18 years in medical writing. They have significant expertise in the strategy and development of regulatory submissions such as Biologics Licensing Applications and Marketing Authorization Applications. Daniel has led medical writing teams, mentored junior personnel, and has hands-on experience crafting clinical and regulatory documents essential for clinical trials. Currently, they are pursuing a Ph.D. in Microbiology and Immunology at Temple University, alongside a Bachelor of Arts in Biological Sciences from the University of Delaware.
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