Over 30 years of clinical research and nursing experience, with the majority of her career consisting of Site management and operations. Jennifer has initiated several clinical trial departments across the US, within academic medical centers, community health systems and private practice settings. She specializes in efficient clinical trial start-up, trial management, training and consulting. Expertise includes protocol feasibility and “fit” for sites, regulatory start-up, budget negotiations/coverage analyses, contract negotiations, education and training of CRCs, CRAs, and PIs, along with SOP development for both sites and IRBs. Jennifer’s clinical research experience spans all therapeutic areas, with various types of sponsors, and in all phases of research, I-IV. Currently serving as a Sr. Director and Principal Consultant for an innovative site management organization working at the intersection of Sites, Sponsors and CROs.