2012 -2016 Executive Director, Global Regulatory Affairs, Early Development and Biomarker Strategy @
2007 -2012 Head of Americas, Regulatory Affairs @
2005 -2007 Regulatory Affairs @
1993 -2005 Regulatory Affairs @
Allison Nance Education
Johns Hopkins University Advanced Academic Programs
Master of Science (Biotechnology)
2015-2017
University of Arizona
Bachelor of Science (BS) (Ecology and Evolutionary Biology)
1991-1992
University of Arizona 1987-1991
Allison Nance Skills
Oncology
Pharmaceutical Industry
Regulatory Submissions
Regulatory Affairs
Clinical Trials
Clinical Development
Biotechnology
Drug Discovery
Medical Devices
Infectious Diseases
Neurology
Healthcare
Commercialization
ICH-GCP
Clinical Research
Biopharmaceuticals
Biomarkers
Cancer
Hardware Diagnostics
Vaccines
Project Management
Management
Ich Gcp
Quality Assurance
Strategy
Regulatory
Research
Business Development
Allison Nance Summary
Allison Nance, based in Cambridge, MA, US, is currently a Senior Vice President, Regulatory Affairs at Lyra Therapeutics. Allison Nance brings experience from previous roles at Jounce Therapeutics, Inc., Celgene Corporation, GE Healthcare and Hoffmann-La Roche. Allison Nance holds a 2015 - 2017 Master of Science in Biotechnology @ Johns Hopkins University Advanced Academic Programs. With a robust skill set that includes Oncology, Pharmaceutical Industry, Regulatory Submissions, Regulatory Affairs, Clinical Trials and more. Allison Nance has 2 emails and 1 mobile phone numbers on RocketReach.
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