Robert Ezzell Email & Phone Number
Director, Global Regulatory Affairs @ Avance Clinical
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Robert Ezzell Location
- Boston, MA, US
Robert Ezzell Work
- 2025 -now Director, Global Regulatory Affairs @
- 2024 -2025 Senior Regulatory Affairs Consultant @ Independent
- 2021 -2023 Senior Director, Regulatory Affairs @
- 2015 -2023 Graduate Instructor-Regulatory Affairs @
- 2019 -2021 Head of Regulatory Affairs @
- 2017 -2019 Associate Director, Global Regulatory Affairs (CMC and Devices) @
- 2015 -2017 Senior Manager, Global Regulatory Affairs (CMC and Devices) @
- 2011 -2015 Regulatory and Quality Engineer @
- 2010 -2011 Global Regulatory Affairs Project Manager @ Shire Human Genetics Therapies (acquired by Takeda)
- 2007 -2010 Principal Scientist (2007-2009); Director, Product Development (2009-2010) @ RenaMed Biologics, Inc (formerly Nephros Therapeutics)
- 2004 -2007 Senior Scientist @ Molecular Geodesics (Tensegra Inc.)
- 1998 -2004 Assistant Professor @ Mass General Hospital - Harvard Medical School
Robert Ezzell Education
- D'Amore-McKim School of Business at Northeastern University
MBA (Operations & Finance)
2006-2007 -
PhD (Cell & Molecular Biology)
- Regulatory Affairs Certification
RAC (Regulatory Affairs Professional Society)
Robert Ezzell Skills
- Combination
- Tissue
- Analytical Processes
- Budgets
- Cost
- Medical Devices
- Finance
- Human Resources
- Reports
- Robust
- Oracle RAC
- Immunity
- Presentations
- Raps
- Electromagnetic Compatibility
- Structure
- Workflow
- Cell
- Obtain
- Project
- Pro*c
- Coordinated
- CMS
- Tissue Engineering
- Surgery
- Unconventional
- ISO 13485
- Directives
- Mdr
- Biology
- Infectious Diseases
- Guidance
- Electrical Safety
- Life Sciences
- Communication
- Conformity Assessment
- Author
- Drug Delivery
- IV
- Protein Purification
- Catheters
- Cell Culture
- Regulatory Requirements
- Agents
- Binding
- Cross Functional Team Leadership
- Conceptual Modeling
- Attachment
- Performance Testing
- Regulatory Submissions
- Home
- Liver
- Status Reports
- Biophysics
- Tests
- Quality System
- Materials
- Driving
- Regulatory Compliance
- Case Studies
- Compilation
- Burns
- CMC
- Institutes
- Assessment
- Chemistry
- Route
- Countermeasures
- Cytokines
- Medical Device Directive
- Health Monitoring
- Prototype
- Concurrent
- Risk
- Research Projects
- Kidney
- Cell Lines
- Nature
- E 3
- Molecular
- Delay
- Teaching
- Regulations
- Strategies
- Strategy
- GMP
- Customer Satisfaction
- Bacterial
- Investigation
- European Union
- Guidelines
- Los Angeles
- Bench
- Remediation
- Regulatory
- Spectroscopy
- Multi User
- Gene Targeting
- Blood Glucose
- Consulting
- Gene Expression
- Project Management
- Sepsis
- Documentation
- Clinical Research
- HPLC
- Hiring
- Filtration
- Phase 1
- Recombinant Dna
- Validation
- Angioplasty
- Contractual Agreements
- Therapists
- Expression
- Image Manipulation
- Wireless
- Microbiology
- Restoration
- Publishing
- Stabilization
- Teacher Training
- Escalation
- Medicine
- Entrepreneurship
- Microscopy
- Stability
- Surveillance
- Hospitals
- Google Groups
- Defense
- Efficacy
- Design
- Scientific
- Biomaterials
- Management
- Biocompatibility
- Purification
- Clinical Trials
- Research
- Sop
- Evaluation
- Producing
- Biotechnology
- Biologics
- Meetings
- Students
- Seminars
- Proposal Writing
- Receptors
- Space
- Institutions
- Threat
- Operations
- Committees
- Cell Biology
- CE marking
- Risk Based Testing
- Drug Eluting Stents
- R&d
- System
- Road
- Business Administration
- Initiation
- Signal
- Insightful
- Extracellular Matrix
- Newton
- Cell Based
- Mechanism of Action
- Mammalian
- Cell Adhesion
- Testing
- Clinical Development
- Business Development
- Data Analysis
- Scholarships
- Conferences
- Immunology
- Animal Models
- qPCR
- Product Development
- GLP
- Regulatory Affairs
- Innovative Solutions
- Biochemistry
- Joint Ventures
- Venture Capital
- Executive Management
- Computed Tomography
- Publications
- Laboratory
- Process Simulation
- Filter
- Bioreactor
- Phase Ii
- Gap Analysis
- Detection
- Ich Gcp
- ICH guidelines
- Treatment
- Strategic Business
- Medical Research
- Quantitative Analytics
- LPS
- Disease
- Software
- Screening
- Customer Service
- Berkeley
- E Business
- Legal
- Fermentation
- Quality Control
- Characterization
- Sentinel
- Deadline Driven
- Advertising Agency
- Document Management
- Risk Management
- Image Analysis
- Manufacturing
- Compliance
- In Vitro
- System Monitoring
- Renal
- Quality Systems
- Purchasing
- Business Alignment
- Fortune
- Thesis
- Boston
- FDA
- Quality Assurance
- cGMP manufacturing
- Strategic Planning
- Databases
- Renal Failure
- Funding
- Portable
- Biomarkers
- Laser
- Qualifying
- PPE
- Wound Care
- Workshops
- Medical Imaging
- Vigilance
- Differentiation
- CAPA
- Responsibility
- Academic
- Throughput
- Unified Communications
- Army
- Renovation
- Affinity Chromatography
- Diagnostics
- Reagents
Robert Ezzell Summary
- Robert Ezzell, based in Boston, MA, US, is currently a Director, Global Regulatory Affairs at Avance Clinical. Robert Ezzell brings experience from previous roles at Independent, atai Life Sciences, Northeastern University and Glympse Bio. Robert Ezzell holds a 2006 - 2007 MBA in Operations & Finance @ D'Amore-McKim School of Business at Northeastern University. With a robust skill set that includes Combination, Tissue, Analytical Processes, Budgets, Cost and more. Robert Ezzell has 2 emails on RocketReach.
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