Training Program Title

Streamline Your Clinical Trial Workload with Effective Project Management

Contributor

Forte MarketingFollow

CTSA Hub Administered

no

Contact Information

marketing@forteresearch.com

Training Program Description

In the clinical research industry, ‘projects’ (i.e. clinical trials) are complex, time-intensive and leave little to no room for error. Particularly when conducting concurrent studies with limited resources, it can be difficult to ensure quality and timely data collection and entry on every study. This can lead to coordinator stress and unhappiness with their job despite the meaningful work they are contributing to better medical research. Clear and effective project management can make or break the success of a clinical trial, and project planning and management are a key part of achieving quality clinical data.

During this webinar, Forte’s Director of Analytics, Wendy Tate, outlines the essential factors of effective clinical trial project management and provide tips to help you successfully manage your individual research portfolio.

Competency Keywords

Clinical research, Clinical trial, Communication, Teamwork, Leadership, Research study management

Digital Commons Disciplines

Medical Education

Public

yes

Cost to Access

no

Competency Domains

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

Learning Objectives

  1. Essential factors of effective clinical trial project management
  2. Best practices for tackling an overwhelming clinical trial workload
  3. Tools to help you streamline cumbersome tasks, such as delegation of authority, document management, and more

Delivery Method

Online

Target Learners

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

Learning Level

Fundamental

Frequency

On demand

Associated Assessment

no

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