Dr. Marta Neve joined Certara in April 2017 as an Associate Director in Integrated Drug Development conducting population PK, PK/PD and exposure-response analyses for regulatory submissions and general drug development support of both small molecules and biologics. Prior to joining Certara, Marta was Associate Director within the Quantitative Clinical Development department in PAREXEL where she conducted modeling and simulation activities in addition to supporting clinical teams as a client-dedicated consultant.
Formerly, Marta was a Principal Pharmacokineticist in the Clinical PK Modeling & Simulation department of GlaxoSmithKline’s Neuroscience R&D Center where she was in charge of the design and quantitative analyses of various Phase 1-3 clinical studies. Over the last 15 years, Marta has been working on a variety of therapeutic areas spanning from psychiatry to neuroscience, oncology, respiratory or rare diseases across all phases of drug development. She is used to working in a multidisciplinary and international environment where excellent communication skills and problem-solving attitudes are imperative.
Marta has a PhD in Engineering with the main focus on modeling and simulation of biological and non-biological data, and an MSc in Computer Science Engineering with a specialization in Biomedics obtained at the University of Pavia (Italy).