Greg Vico
Executive Director, Clinical Quality Assurance @ ADC Therapeutics
About
I am passionate about advancing science and medicine. My mission is to foster a culture of quality and continuous improvement leveraging my 25 years of experience at J&J, BMS and Charles River Laboratories. I pride myself on collaboration, applying best practices and standards, and delivering high-quality products and services that meet the needs of patients and regulators.
United States
New York City Metropolitan Area
Pharmaceuticals
Clinical Trials, Quality Assurance, Pharmaceutical Industry, Lifesciences, Sop, GLP, FDA, Clinical Research, Cross-functional Team Leadership, Biotechnology, Project Management, Healthcare, GMP, CRO, Leadership, Management, Regulatory Affairs, Validation, Change Control, Life Sciences
Experience
Executive Director, Clinical Quality Assurance
ADC Therapeutics
New Providence, New Jersey, United States
Founder / Principal Consultant
Pharma Quality Insights, LLC
New Jersey, United States
At Pharma Quality Insights, LLC, I lead quality assurance strategy and execution for organizations navigating the complex regulatory landscape of the pharmaceutical and biotech industries. I partner with small and large pharma companies, biotech firms, CROs, and clinical investigator sites to strengthen their quality systems through: Inspection preparation GCP/GLP audits QMS GAP analysis Due diligence, integration, and acquisition support Fractional quality leadership My focus is helping clients build sustainable compliance frameworks and operational resilience that drive both regulatory success and business growth.
Member of Engaging Stakeholders in Trial Design
Clinical Trials Transformation Initiative (CTTI)
Providing Input to Project as Sponsor Stakeholder Presented @ Multi-Stakeholder Expert Meeting in Washington DC (Apr 2023)
Sr. Director, Process Quality, Research & Development Quality
Bristol Myers Squibb
Lead Root Cause Investigation Team Oversee Serious Breach Process Lead a team of Process Quality Professionals who oversee critical Clinical Processes at BMS
Mirati & Karuna R&D Quality Integration Lead
Bristol Myers Squibb
Sr. Director, Therapeutic Area Quality, Research & Development Quality
Bristol Myers Squibb
Director - Quality Planning and Strategy, Immunology, Infectious Disease, & Vaccines TA
Johnson & Johnson
NJ
Director, Strategic Development QA
Johnson & Johnson
Associate Director, Clinical QA, R&D Quality & Compliance
Johnson & Johnson
Manager, Therapeutic Area Clinical QA
Johnson & Johnson Innovative Medicine
Raritan
Program Manager Clinical Quality Assurance
Johnson & Johnson Innovative Medicine
Senior Specialist Clinical Quality Assurance
Johnson & Johnson
Senior Specialist Pre-clinical Quality Assurance
Johnson & Johnson
Senior Associate Pre-clinical Quality Assurance
Johnson & Johnson
Quality Assurance Specialist
Charles River Laboratories
Pre-clinical Quality Assurance Associate
Charles River Laboratories
Pre-clinical Laboratory Technician
Charles River Laboratories
Education
Delaware Valley University
Biology, General
Minor in Computer Information Systems Management
Delaware Valley University
Business Administration and Management, General
15 credits in Business Administration completed post graduation
Temple University
Quality Assurance / Regulatory Affairs
Greg Vico's Contact Information
Phone
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