Lisa Pitt Email & Phone Number

Senior Vice President Regulatory Affairs @ Jasper Therapeutics

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Lisa Pitt Location

Washington, DC, US

Lisa Pitt Work

Senior Vice President Regulatory Affairs @ (September 2026 - Present)
Vice President, Head of Regulatory Affairs @ (January 2024 - May 2024)
Head Of Regulatory Affairs @ NorthSea Therapeutics (August 2022 - December 2023)
Vice President, Head Of Regulatory Affairs @ (May 2021 - June 2022)
Vice President, Head of Regulatory Affairs @ (March 2018 - May 2021)
Vice President, Global Regulatory Affairs @ (March 2016 - August 2017)
Senior Regulatory Health Project Manager @ (April 2015 - March 2016)
Director, Global Regulatory Affairs @ (September 2009 - April 2015)
Associate Director, Drug Regulatory Affairs @ (June 2008 - September 2009)
Director, Drug Development Consultant @ (September 2007 - January 2008)
Senior Associate Director, Drug Regulatory Affaris @ (March 2005 - September 2007)
Associate Director @ (January 2001 - January 2004)

Lisa Pitt Education

Seton Hall University School of Law
Master of Science Jurisprudence (Health Law & Policy)
2004-2006
University of Maryland Baltimore
Doctor of Pharmacy (PharmD)
1994-1998

Lisa Pitt Skills

Regulatory Intelligence
Marketing Authorisation Application (MAA)
Research and Development (R&D)
Regulatory Policy
Regulatory Strategy
Change Management
Clinical Development
Regulatory Affairs
Regulatory Submissions
IND
Pharmaceutical Industry
Drug Development
Clinical Trials
Biotechnology
Biopharmaceuticals
FDA
eCTD
Biologics
Clinical Research
Therapeutic Areas
GMP
Infectious Diseases
Drug Discovery
CRO
GCP
CTMS
Vaccines
Medical Affairs
Technology Transfer
GLP
Sop
Pharmacovigilance
Medical Writing
21 CFR Part 11
Clinical Study Design
Immunology
Lifesciences
Validation
Regulatory Requirements
NDA
Life Sciences
Customer Service
Research
Marketing
Sales
New Market
ELISA
Spl
Phase 2
Supplements
Metabolism
CTAs
Analysis
Policy
Supervision
EMA
External Clients
Regulatory Expertise
Central Nervous System
Pacific
GAP
Product Reviews
Diabetes
Vendors
Gross Margin
Phase
Branding
Pharmaceutical Product Development
New Business Development
Latin America
Investigation
Regulations
Stage
Regulatory Compliance
Diagnostics
CTA
Manuals
Advertising Agency
Regulatory Agencies
Schedules
Stakeholders
Drug Product
Six Sigma
Subject Matter Expert
Project Staffing
Promotional
Strategic Marketing
Operational Support
Pls
Jersey
Training
Drug Interactions
European Union
Ddmac
Quality Assurance
Communication
Hematology
Conveying
Broad Experience
Toxicology
Hospitals
International
Regulatory Knowledge
Amendments
Business Initiatives
Forms
Committees
Obesity
Utilization
Sage Act
FIX Protocol
Biology
Wood
Oversight
Tests
Oncology
Biotechnology Industry
Materials
Outline
Dia
Snda
Business Process
Pediatrics
Negotiation
Internal Compliance
Revenue
Expedited
Pharmacy
Treatment
Business Development
Project Bidding
Compliance
Assessment
Resolve
Part Time
Designations
Public Speaking
Knowledge Base
Package Inserts
Margin Improvement
Asia
Co Development
Modernization
PowerPoint
Monitors
Coordinate
Microbiology
Filing
In Vitro
HIV
Laboratory
Cardiovascular
Baltimore
Legal Advice
Structured Finance
Applications
Acting
Evaluation
Phase 1
Clinical Pharmacy
Rolling
Chemical
Coordination
Execution
Documentation
Dra
Trade Associations
Project Planning
Timelines
Fibrosis
Product Development
Mortality
Organizational Structure
Diligent
Budgeting
Operating Expenses
Microsoft Office
Guidance
Home
Sensitivity
Aol
Japan
Coordinated
Patient Outcomes
Customer Satisfaction
Coaching
Gene Therapy
Source
CPIM
Early Development
Health Outcomes
Medical Devices
Europe
Health Law
New Process
Proof of Concept
Project Management
Executive Management
Active
Patient
Internal Audit
Strategies
Limits
Therapists
Legislation
Testing
Design
Atherosclerosis
Management
Supplemental
Biosimilars
Implementation Plans
Regulatory Science
Dyslipidemia
Pharmaceutics
Global Health
Hypertension
Nursing
Gastroenterology
Cross Functional Team Leadership
Advertising
Project Teams
Market
Cycle Time Reduction
Qualify
Delaware
Ndas
Programmatic
Written
Case Management
Strategy
Canada
Optimization
Evidence
Project
Briefing
Development of Promotional Materials
Meetings
Streamline
Food and Drug Law
Mentoring
Healthcare
Role Modeling
Draft
Switzerland
Serving
Training Manuals
Staff Development
Plates
Novartis
Respiration
Silver
Proposal Writing
Western Blotting
Disease
Labelling
Due Diligence
Quality Control
Product Life Cycle
Reports
System Monitoring
Electronics
Scientific
Interpreting
Strategist
Human Resources
Revision
Endocrine
Profit
Antigen
Physicians
Consulting
Career Development
Deviations
Payer
Qualification
Efficiencies
Legal
Demonstration
Project Reviews
Contractual Agreements
Staff Retention
Bronze
Inactive
Rare
Raw Materials
Budgets
New Initiatives
Responsibility

Lisa Pitt Summary

Lisa Pitt, based in Washington, DC, US, is currently a Senior Vice President Regulatory Affairs at Jasper Therapeutics/Kira Pharmaceuticals. Lisa Pitt brings experience from previous roles at Aiolos Bio, NorthSea Therapeutics, Horizon and Viela Bio. Lisa Pitt holds a 2004 - 2006 Master of Science Jurisprudence in Health Law & Policy @ Seton Hall University School of Law. With a robust skill set that includes Regulatory Intelligence, Marketing Authorisation Application (MAA), Research and Development (R&D), Regulatory Policy, Regulatory Strategy and more. Lisa Pitt has 1 emails and 3 mobile phone numbers on RocketReach.

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