On-Demand Webinar: How to Develop a Global Clinical Study Budget Like a Pro

Control your budgets and win

 

Clinical research is a notoriously cost-sensitive industry. The Tufts Center for the Study of Drug Development estimated the average cost of bringing a new drug to market to be over $2 billion – and with clinical trial costs on the rise, it’s more important than ever to take a smart approach to developing your study budgets. This is especially true when taking on global clinical trials.

Join Débora S. Araujo, founder and CEO of the pharmaceutical skill development company ClinBiz, will offer organizations conducting clinical trials insight into a host of critical issues related to various aspects of clinical study budgets, and will be a key resource for any organization looking to increase the cost-efficiency of their clinical trials.
  • What questions to ask yourself during the clinical study budget development stage to avoid pushback from senior management at the budget approval stage
  • What to include in your clinical study budget package so your budget gets approval quickly
  • How to use benchmarks to achieve bulletproof clinical study budget estimates
In the current environment, organizations must do whatever possible to mitigate the costs of bringing new products to market approval. What approach will you take to budget planning in your next study?
Presented by
Débora S. Araujo

Founder & CEO, ClinBiz

 

Débora S. Araujo has over a decade of experience in the pharmaceutical industry working and consulting for Fortune 500 companies. Her focus is on the business aspects of clinical trials, including clinical contracting and financial management, clinical outsourcing and CRO/vendor management, global clinical trial budgeting and forecasting, clinical financial analytics and metrics/KPIs, site budget development and negotiations, fair market value and global investigator site payments. She has utilized her expertise to drive change in the industry via thought leadership material, conference presentations and consulting engagements. Débora’s passion for driving practical change in the industry led her to launch ClinBiz, an online platform where clinical research professionals can stay connected and updated on the latest topics, trends and technologies related to the business aspects of clinical trials. Débora is also the author of the bestselling book, “The Four Villains of Clinical Trial Agreement Delays and How To Defeat Them.”



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