Nicole Hurst Email and Phone Number
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• Board Certified Toxicologist with 15+ years of industry experience• Experience across drug development process• Experience in the therapeutic areas of Oncology, Inflammation, Pain, and Ophthalmology• Experience managing cross-functional groups• Excellent written and communication skills, experience writing many regulatory documents• Ability to manage many tasks at once and to produce quality work in a timely manner
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Toxicology Senior Research FellowVertex Pharmaceuticals 2021 - PresentBoston, Ma, Us -
Fellow IiVertex Pharmaceuticals Aug 2019 - 2021Boston, Ma, Us -
Fellow I, Preclinical Safety AssessmentVertex Pharmaceuticals Sep 2016 - Aug 2019Boston, Ma, Us• Design, implement, analyze and interpret GLP toxicology studies conducted externally to support programs in multiple therapeutic areas• Manage Contract Research Organization relationships, study monitoring and report coordination • Write and review nonclinical safety assessment sections of regulatory documents for worldwide submission (IND/CTA, NDA, etc)• Represent Vertex in meetings with regulatory authorities regarding nonclinical safety assessments.• Toxicology representative on multi-disciplinary product development teams• Collaborate with discovery research on toxicity issues during lead candidate evaluation and selection • Knowledge of both GLP and relevant global regulatory guidance and regulations• Participate in diligence activities related to partnering/licensing -
Research DirectorInfinity Pharmaceuticals Dec 2007 - Aug 2016Cambridge, Massachusetts, Us• Design, implement, analyze and interpret GLP toxicology and safety pharmacology studies conducted externally to support programs in multiple therapeutic areas• Manage Contract Research Organization relationships, study monitoring and report coordination • Write and review nonclinical safety assessment sections of regulatory documents for worldwide submission (IND/CTA, NDA, etc)• Represent Infinity in meetings with regulatory authorities regarding nonclinical safety assessments.• Lead cross functional team to take compound from development candidate stage to first in human trial• Toxicology representative on multi-disciplinary product development teams• Develop protocols and conduct in -house exploratory toxicology studies • Collaborate with discovery research on toxicity issues during lead candidate evaluation and selection • Knowledge of both GLP and relevant global regulatory guidance and regulations• Participate in diligence activities related to partnering/licensing• Represent Infinity as a member of Technology Evaluation Consortium responsible for evaluating new toxicology tools/assays -
Research Associate Director, ToxicologyInfinity Pharmaceuticals Jul 2009 - Jul 2015Cambridge, Massachusetts, Us• Same duties as described in Research Director position -
Lead Senior Scientist, ToxicologyInfinity Pharmaceuticals Dec 2007 - Jul 2009Cambridge, Massachusetts, UsSimilar duties to those described for Research Director -
Associate Director Of Preclinical DevelopmentOxigene, Inc. Jun 2005 - Dec 2007• Direct in vivo and in vitro efficacy, pharmacodynamic, and pharmacokinetic studies with lead compounds in academic settings and using outsourced vendors in the therapeutic areas of oncology and ophthalmology• Design and supervise toxicology assessments of lead compounds• Responsible for the preclinical and safety assessment sections of regulatory submissions, study reports and manuscripts• Serve as an expert on safety issues for in-house and collaborative projects• Participate in partnering/licensing and acquisition of OXiGENE's therapeutics• Represent OXiGENE in meetings with regulatory authorities regarding preclinical and safety assessments.• Build cross-functional collaborations and effectively manage vendors • Prepare departmental budgets and forecast department spending for programs • Knowledge of both GLP and relevant global regulatory guidance and regulations
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Scientist And Program ManagerCombinatorx Inc Aug 2000 - Jun 2005As an early employee of this start up, worked as a lead development scientist, worked in regulatory/clinical development, and program management. More details can be provided on request.
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Postdoctoral ResearcherHarvard T.H. Chan School Of Public Health Feb 2000 - Aug 2000Boston, Massachusetts, Us• Examined restriction enzyme-mediated integration of plasmid DNA into embryonic stem cells using cell lines derived from knockout mice. • Investigated levels of homologous versus illegitimate recombination in cell lines with mutations in DNA repair genes. • Developed assay to detect genetic deletions induced by toxicants in a novel mouse model
Nicole Hurst Skills
Nicole Hurst Education Details
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University Of North Carolina At Chapel HillToxicology -
University Of North Carolina At Chapel HillGeneral
Frequently Asked Questions about Nicole Hurst
What company does Nicole Hurst work for?
Nicole Hurst works for Vertex Pharmaceuticals
What is Nicole Hurst's role at the current company?
Nicole Hurst's current role is Fellow II, Preclinical Safety Assessment at Vertex Pharmaceuticals.
What is Nicole Hurst's email address?
Nicole Hurst's email address is ni****@****nfi.com
What is Nicole Hurst's direct phone number?
Nicole Hurst's direct phone number is (617)-301*****
What schools did Nicole Hurst attend?
Nicole Hurst attended University Of North Carolina At Chapel Hill, University Of North Carolina At Chapel Hill.
What skills is Nicole Hurst known for?
Nicole Hurst has skills like Toxicology, Drug Discovery, Drug Development, Pharmaceutical Industry, Medical Writing, Regulatory Submissions.
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