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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.