Michael Agard Email & Phone Number

Principal Consultant @ Epista Life Science

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Michael Agard Location

Philadelphia, PA, US

Michael Agard Work

2024 -now Principal Consultant @
2022 -2024 Director Clinical Consulting @
2021 -2022 Managing Consultant @
2010 -2021 Director, Consulting Expert @ CGI

Michael Agard Education

Penn State Great Valley
MLD (Master of Leadership Development)
2006-2008
University of Connecticut
BS (Pharmacy)
1978-1981

Michael Agard Skills

Proposal Writing
Warehouse Operations
Microsoft Outlook
Negotiation
Marketing Strategy
Microsoft Word
Management
Key Performance Indicators
Team Leadership
Jira
Inventory Management
Manufacturing Process Improvement
Sales
Good Manufacturing Practice (GMP)
Leadership
Forecasting
Organizational Development
Research and Development (R&D)
Supply Chain Management
Team Building
Microsoft PowerPoint
Mergers & Acquisitions (M&A)
Business Management
Manufacturing Operations Management
Software Development Life Cycle (SDLC)
Business Analytics
IT Service Management
CRF design
Pharmacovigilance
Clinical Research
Software Quality Assurance
IT Management
CDISC Standards
U.S. Food and Drug Administration (FDA)
Software Development
Data Analysis
Change Control
Software Testing
Business Strategy
Regulatory Submissions
Microsoft Office
Clinical Monitoring
Data Integration
Data Management
Business Process Analysis
Systems Analysis
Drug Development
English
System Requirements
Documentation
Communication
Business Systems Analysis
User Acceptance Testing
CRO Management
Data Analytics
Business Requirements
Business Process
Electronic Trial Master File (eTMF)
Analytical Skills
Clinical Operations
Business Analysis
Clinical Trials
Veeva
Consulting
Document Management
Change Management
Process Improvement
Validation
21 CFR Part 11
Strategy
IT Strategy
Optimization
Requirements Gathering
Good Clinical Practice (GCP)
Regulatory Affairs
Project Management
Data Migration
Reporting & Analysis
Business Process Improvement
Electronic Data Capture (EDC)
Standard Operating Procedure (SOP)
Pharmaceutical Industry
Clinical Development
Software Documentation
Analytics
Business Process Design
Management Consulting
Clinical Trial Management System (CTMS)
eTMF
Visio
Microsoft Excel
Organizational Effectiveness
Leadership Development
Compliance
Trial Master File
Software Implementation Management
Computer Software Training
probem solving
Computer System Validation
CTMS
SharePoint
Cross-functional Team Leadership
GCP
SOP
EDC
GMP
FDA
Quality Assurance
SDLC
Quality System
Quality Systems
Portal Technologies
Identity Management
Writing
Quality Management
Clinical Trial Management System Ctms
Supplies
Ich Gcp
Printing
Citrix
Shipping
Reporting Systems
Vendors
Reporting and Analysis
Data Entry
Rdc
Net
Clinical Data Management
GxP
Good Clinical Practice Gcp
Structure
Road
Taxonomy
Cross Functional Team Leadership
Batch Processing
Eroom
Articulate Studio
Packing
u.s. Food and Drug Administration Fda
Traceability
Regulatory Compliance
eCRF
Webinars
Ecopy
Digital Signatures
Design
Standard Operating Procedure Sop
Science
Security
File
Metrics
PowerPoint
Monitors
Workflow
Human Resources
Pennsylvania
Networking
Process Validation
System
Cell
FrontPage
Reports
CVS
Learning Management Systems
Pharmaceutical Sciences
Lifesciences
Testing
Business Efficiency
Training
Microsoft Office Sharepoint Server
Microsoft Publisher
Centra
Scheduling
System Monitoring
Reporting
Commercial Real Estate
Investigation
MapPoint
R&d
Hardware
Billing Systems
Visionary
Information Technology
SAP
Professional Associations
Iiba
Trials
RFP
Adverse Events
Technology Implementation
Schedules
Home
IV
Life Sciences
System Administration
User Requirements
Crfs
Operations
Clinical Data
Clinical Trial Management
WebEx
Maps
Captivate
Digital Signage
Indexing
Business Intelligence
Microsoft Project
Project Planning
Documentum
Kofax
Project
Contractual Agreements
House
Information Architecture
Pharmacy
Electronic Data Capture Edc
Business Process Mapping
Paper
Presentations
Software Development Life Cycle Sdlc
Responsibility
Six Sigma
Project Teams
Packaging
Regulations
Multi Disciplined
Labelling
International
Data Warehousing
Inventory System
Portals
Scope Management
Electronics
ICH guidelines
Adobe Connect
Software
E Learning
Oracle
Business Objects
Process Mapping
PMI
IVR
Clinical
Good Manufacturing Practice Gmp
Scanners
Risk
Business Intelligence Bi
Connecticut
Filing
Inclusion
Templates
Supply Chain
Diagrams
System Deployment
Automation
Electronic Data Capture
Clinical Trial Management System
Good Clinical Practice
u.s. Food and Drug Administration
Standard Operating Procedure
Software Development Life Cycle
Good Manufacturing Practice

Michael Agard Summary

Michael Agard, based in Philadelphia, PA, US, is currently a Principal Consultant at Epista Life Science. Michael Agard brings experience from previous roles at NNIT and CGI. Michael Agard holds a 2006 - 2008 MLD in Master of Leadership Development @ Penn State Great Valley. With a robust skill set that includes Proposal Writing, Warehouse Operations, Microsoft Outlook, Negotiation, Marketing Strategy and more. Michael Agard has 4 emails and 2 mobile phone numbers on RocketReach.