Jack Lott Email & Phone Number
Director, Clinical Safety and Pharmacovigilance @ Pyxis Oncology
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Jack Lott Location
- Toms River, NJ, US
Jack Lott Work
- Director, Clinical Safety and Pharmacovigilance @ (March 2026 - Present)
- Director, Pharmacovigilance Scientist @ (February 2025 - November 2025)
- Safety Scientist, Immunology and Inflammation, Global Patient Safety @ (May 2022 - January 2025)
- Associate Director, Lead, Global Risk Management Strategy, Patient Safety and Epidemiology @ (November 2019 - December 2021)
- Manager, Global Risk Management Strategy and Policy @ (August 2017 - November 2019)
- Manager, REMS Programs @ (March 2014 - August 2017)
- Project Manager @ (June 2010 - March 2014)
- Assistant Manager, Molecular Imaging and Biomarkers @ CoreLab Partners, Inc. (formerly RadPharm) (December 2008 - June 2010)
- Assistant Project Manager, Clinical Operations @ CoreLab Partners, Inc. (formerly RadPharm) (April 2008 - December 2008)
- Project Leader, Clinical Operations @ CoreLab Partners, Inc. (formerly RadPharm) (April 2007 - April 2008)
- Project Coordinator, Clinical Operations @ CoreLab Partners, Inc. (formerly RadPharm) (August 2006 - April 2007)
- Laboratory Intern @ (May 2005 - August 2005)
Jack Lott Education
- Seton Hall University
Ph.D Student (School of Health and Medical Sciences)
- The Johns Hopkins University
Master of Science - MS (Biotechnology)
- Ramapo College of New Jersey
Bachelor of Science - BS (Biology)
Jack Lott Skills
- Safety Regulations
- Leadership
- Patient Safety
- Pharmacovigilance
- Risk Management
- REMS
- Strategic Planning
- Scientific Writing
- Scientific Presentation
- Good Pharmacovigilance Practice (GVP)
- Regulatory Submissions
- Regulatory Compliance
- Regulatory Reporting
- Presentations
- Creative Strategy
- Argus Safety
- Adverse Event Reporting
- MedDRA
- Clinical Trials
- Health Policy
- Protocol Development
- Vendor Audit
- Logistics Management
- U.S. Title 21 CFR Part 11 Regulation
- Product Strategy
- Medical Imaging
- Vendor Partnerships
- Data Exchange
- Molecular Imaging
- CDISC Standards
- Laboratory Analysis
- Start-up Ventures
- Team Organization
- Cross-functional Coordination
- E2B
- KAB
- Business Alliances
- SUSAR
- DSUR
- PBRER
- Risk Management Plans (RMP)
- Reporting Requirements
- Interpersonal Communication
- Adverse Events
- Pharmaceutical Industry
- Biotechnology
- Project Management
- Agile Methodologies
- Quality Assurance
- Cross-functional Team Leadership
- Drug Development
- RECIST
- Regulatory Affairs
- GCP
- CRO
- Standard Operating Procedure (SOP)
- Data Management
- Electronic Data Capture (EDC)
- Data Analysis
- Strategy
- Account Management
- Analytical Skills
- Team Leadership
- Management
- Electronic Common Technical Document (eCTD)
- Time Management
- Customer Service
- Project Coordination
- Presentation Skills
- Budgeting
- Vendor Management
- ETASU
- FDA Guidance for Industry
- Relationship Building
- Strategic Communications
- Business Relationship Management
- Microsoft Excel
- Microsoft Word
- Microsoft PowerPoint
- Medical Writing
- PSUR
- U.S. Food and Drug Administration (FDA)
- Public Policy
- Compliance Management
- Communication
- Cardiac Monitoring
- Data Entry
- Laboratory Techniques
- Good Laboratory Practice (GLP)
- Mass Spectrometry
- NMR Spectroscopy
- UV/Vis Spectroscopy
- Environmental Science
- OSHA Compliance
Jack Lott Summary
- Jack Lott, based in Toms River, NJ, US, is currently a Director, Clinical Safety and Pharmacovigilance at Pyxis Oncology. Jack Lott brings experience from previous roles at Cullinan Therapeutics, Regeneron and Celgene. Jack Lott holds a Ph.D Student in School of Health and Medical Sciences @ Seton Hall University. With a robust skill set that includes Safety Regulations, Leadership, Patient Safety, Pharmacovigilance, Risk Management and more. Jack Lott has 2 emails and 1 mobile phone numbers on RocketReach.
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