Douglas Lane, MS has a strong background in regulatory affairs, clinical research, and program management. With experience in coordinating clinical trials, managing regulatory submissions, and providing strategic recommendations to development teams, Douglas has a well-rounded skill set in the healthcare and pharmaceutical industry. With a Master of Science degree in Regulatory Affairs and a Bachelor of Science in Neuroscience, Douglas brings a unique perspective to their role as a Senior Regulatory Affairs Manager at Candel Therapeutics.
March 1, 2024 - present
March, 2023
September, 2022
April, 2021
September, 2020
January, 2019