Sarah Voytek
Vice President, Translational Medicine & Global Program Lead @ nChroma Bio
About
Drug developer with proven leadership, collaboration and communication skills – leveraging expertise in innovative pharmaceutical development to address unmet medical need.
United States
Greater Boston
Biotechnology
Biochemistry, In Vitro, Molecular Biology, Protein Purification, Protein Chemistry, Drug Discovery, Life Sciences, Biotechnology
Experience

Senior Director, Non-clinical & Translational Development and Program Leader
Cambridge, Massachusetts, United States
• Develop and oversee nonclinical & translational strategy of an autologous TCR Treg cell product for progressive multiple sclerosis • Establish relationships with academic scientists, contract research organizations and consultants to support pipeline programs

Director, Preclinical & Translational Development
Cambridge, MA
• Led Preclinical & Translational Development department in Severe Genetic Disease business unit supervising staff of Strategy Leads, Pharmacologists, Research Associates and a CRO Program Manager • Formalized translational science framework supporting late-stage clinical development and led Lenti- D and Zynteglo translational science teams • Monitored integrated pharmacology, efficacy and safety data across clinical programs • Investigated clinical safety events leading to regulatory submissions and scientific publications

Associate Director, Preclinical & Translational Development
Cambridge, MA
• Led Preclinical & Translational Development Program Strategy team overseeing nonclinical development for bluebird bio pipeline programs – early research through Phase III clinical development • Engaged in INTERACT and pre-IND meetings with FDA on the development of gene-edited CAR T and HSC gene therapy products • Presented research data and nonclinical strategy considerations at scientific meetings and industry consortia

Senior Investigator I, Preclinical Safety
Cambridge, MA
• Preclinical safety lead for programs in Cardiovascular & Metabolism, Infectious Disease, Neuroscience and Oncology disease areas • Designed and executed submission-enabling nonclinical development studies • Supported strategic portfolio acquisition and disposition of preclinical/clinical assets via due diligence opportunities • Drove the adoption of advanced microscopy techniques for in vitro and in vivo investigative safety applications

Investigator II, Preclinical Safety
Cambridge, MA
• Managed an investigative toxicology research laboratory to contextualize safety findings, support regulatory submissions and address health authority requests • Designed and directed preclinical studies in collaboration with internal and CRO teams
Sarah Voytek's Contact Information
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