Laurel is a highly skilled clinical development and operations professional with over 20 years of experience. She excels in functional area oversight, clinical study/program management, and monitoring/site management. Laurel has a proven track record in leading Phase I to IV clinical trials across a broad range of therapeutic areas, including first-in-human studies, ADME, drug-drug interaction, bioequivalence, QTc, and pharmacokinetic studies.…

Precision, expertise, and dedication define Meg’s work as a clinical operations consultant at Blue Parachute. With strengths in site management, TMF rescue and organization, document development, and process improvements, she ensures every clinical trial story is a success. With a passion for efficiency and a knack for identifying gaps and trends, Meg is committed to delivering high-quality results. Off the…