Training Program Title

How Centralizing Research Operations Can Streamline Your Clinical Trials

Contributor

Forte MarketingFollow

CTSA Hub Administered

no

Contact Information

marketing@forteresearch.com

Training Program Description

As the clinical research industry strives to achieve new efficiencies, we’ve seen a shift in the way research institutions are organized. More and more institutions are working to centralize their trial operations. A central clinical trials office (CTO) can standardize key processes and workflows by addressing operational hurdles at a high level within the organization. These include negotiations, billing & regulatory compliance and budgeting, just to name a few.

Northwell Health’s Vice President of Clinical Research, Christina Brennan discusses the benefits of centralization and key points to consider when centralizing and standardizing your research operations.

Competency Keywords

Clinical research, Clinical trial, Billing, Budget, Negotiation

Digital Commons Disciplines

Medical Education

Public

yes

Cost to Access

no

Competency Domains

Clinical Trials Operations; Study and Site Management; Communication and Teamwork

Learning Objectives

  1. Why centralization is an important step to streamline processes
  2. Opportunities where a centralized approach could be beneficial, including study activation
  3. Steps to generate buy-in throughout your organization, including leadership

Delivery Method

Online

Target Learners

Principal Investigators; Clinical Research Professionals (other than PI); Undergraduate, graduate or professional degree students; Community Partners

Learning Level

Fundamental

Frequency

On demand

Associated Assessment

no

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