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
Billing Compliance: Foundations Class
How to Explain Study Costs & Billing to Patients
Tools and Techniques for Study Budget Negotiation Prep
Hidden Costs in Clinical Trials: Identifying & Negotiating
Creating the Medicare Coverage Analysis
Oncology Trials: Budget & Billing Best Practices
Sponsor Perspective: Challenges of Creating Study Budgets
Are Sites Chasing Money or Chasing Tails? Best Practices for Site Payments
Advanced Research Billing Compliance Topics
FDA Audits & 483 Responses
Is it All Just Copy & Paste? (Pros & Cons of Repeat Business Between Sponsors & Sites)
Innovative Methods of Assessing Protocol & Site Feasibility
Medical Device Trials: Similarities & IMPORTANT Differences
Patient Reimbursements: Regulations, Ethics, and Real World Challenges
Site Metrics: What Are You Measuring
Study Pipelines: Identifying and Securing Study Opportunities
Auditing and Monitoring
MCA Support Services: Buy or Build?
Fair Market Value in the Age of Price Transparency
Selling Your Leadership on the Value of Clinical Trials Research
How to Explain Study Costs & Billing to Patients
Tools and Techniques for Study Budget Negotiation Prep
Hidden Costs in Clinical Trials: Identifying & Negotiating
Creating the Medicare Coverage Analysis
Oncology Trials: Budget & Billing Best Practices
Sponsor Perspective: Challenges of Creating Study Budgets
Are Sites Chasing Money or Chasing Tails? Best Practices for Site Payments
Advanced Research Billing Compliance Topics
FDA Audits & 483 Responses
Is it All Just Copy & Paste? (Pros & Cons of Repeat Business Between Sponsors & Sites)
Innovative Methods of Assessing Protocol & Site Feasibility
Medical Device Trials: Similarities & IMPORTANT Differences
Patient Reimbursements: Regulations, Ethics, and Real World Challenges
Site Metrics: What Are You Measuring
Study Pipelines: Identifying and Securing Study Opportunities
Auditing and Monitoring
MCA Support Services: Buy or Build?
Fair Market Value in the Age of Price Transparency
Selling Your Leadership on the Value of Clinical Trials Research