Our Team

Neha joined Biologics Consulting in January 2025, leveraging nearly four years of experience as a nonclinical Study Director at leading Contract Research Organizations (CROs), Charles River Laboratories and Altasciences. In these roles, she served as the primary liaison for clients, overseeing GLP and non-GLP nonclinical studies, including IND-enabling programs for both small and large molecules across various therapeutic areas and species. She collaborated with clients to design customized protocols, monitor study progress, and draft nonclinical study reports while working closely with internal and external teams to achieve key deliverables and milestones. In addition to her technical expertise, Neha has contributed to the training and mentoring of new Study Directors and students, fostering a collaborative and supportive learning environment. She also served on the Institutional Animal Care and Use Committee (IACUC), where she participated in protocol development and compliance initiatives. Neha holds a Ph.D. in Pharmaceutical Sciences, where her research focused on neuropharmacology and neurotoxicology. Her dissertation assessed the therapeutic potential of compounds for central nervous system (CNS) disorders and investigated the neurotoxic effects of stimulants, including synthetic cathinones. At Biologics Consulting, Neha applies her background in nonclinical study management and regulatory compliance to support clients. As an Associate Consultant, she collaborates with senior and principal-level consultants on multidisciplinary teams, ensuring clients achieve regulatory success and advance their development programs. Education: Ph.D., Pharmaceutical Sciences, Mercer University, College of Pharmacy, Atlanta, GA (2021) Bachelor of Pharmacy (B. Pharm.), Institute of Chemical Technology, Mumbai, India (2017).