
Full Name
Geoffrey Schick
Job Title
Director, Strategic Site Partnerships
Company
WCG
Speaker Bio
Clinical trials research professional with 20+ years of experience leading research departments/institutes for a variety of healthcare organizations. Have helped both national and regional integrated healthcare delivery systems to create centralized clinical trials offices, and to improve performance financially and operationally. Currently working to expand WCG's Site Network to community-based cancer providers, and ensure Investigators have access to industry-sponsored trials to offer their patient base. Certified in Healthcare Research Compliance through HCCA / SCCE.
Speaking At
Block by Block: Building Research Billing into the Revenue Cycle
Billing Compliance & Medicare Coverage Analysis
Developing a Site Budget from Protocol
Study Budget Negotiation: Tips & Tricks
Making Sure Your MCA is Put into Practice
Accelerating Activation with AI: Budgets & Medicare Coverage Analysis
Sponsor Perspective on Study Budgets & Negotiation
Best Practices for Best Budgets
Research Compliance Basics: Anti-Kickback, Stark, and False Claims
Supercharge Your Site's Success: Billing Compliance for Investigational Device Trials
Panel Discussion: Managing a Successful Study Opportunity Pipeline
AI & Clinical Trial Budgeting
Medicare Reimbursement for Clinical Trials
Billing Compliance & Operations
Growing a Research Program & Staffing Challenges
Addressing (& Preventing) Investigator Burnout
Panel Discussion: Advanced MCA & Stump the (Billing) Experts
RBC Auditing & Clinical Documentation
Panel Discussion: Study Budgets - Pricing and Fair Market Value
Justifying the Value of Clinical Trials Research to C-Suite
Billing Compliance & Medicare Coverage Analysis
Developing a Site Budget from Protocol
Study Budget Negotiation: Tips & Tricks
Making Sure Your MCA is Put into Practice
Accelerating Activation with AI: Budgets & Medicare Coverage Analysis
Sponsor Perspective on Study Budgets & Negotiation
Best Practices for Best Budgets
Research Compliance Basics: Anti-Kickback, Stark, and False Claims
Supercharge Your Site's Success: Billing Compliance for Investigational Device Trials
Panel Discussion: Managing a Successful Study Opportunity Pipeline
AI & Clinical Trial Budgeting
Medicare Reimbursement for Clinical Trials
Billing Compliance & Operations
Growing a Research Program & Staffing Challenges
Addressing (& Preventing) Investigator Burnout
Panel Discussion: Advanced MCA & Stump the (Billing) Experts
RBC Auditing & Clinical Documentation
Panel Discussion: Study Budgets - Pricing and Fair Market Value
Justifying the Value of Clinical Trials Research to C-Suite