CenterWatch Announces — Best Practices for Clinical Trial Site Management Report

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Clinical trial professionals: take one’s clinical trial management skills and career to the next level with these best practices. Order now.

WCG CenterWatch

WCG CenterWatch

Best Practices for Clinical Trial Site Management
CenterWatch Management Report

Clinical trial professionals must know how to do it all: engage patients, maintain investigational drug accountability, monitor and ensure data integrity, use electronic data and document storage systems, and investigate the root cause of trial problems.

Get hands-on, in-depth guidance with the Best Practices for Clinical Trial Site Management, which explains how to perform a variety of practical job responsibilities so one can more effectively manage and execute clinical trials. It shares the latest thinking on best practices for must-know topics, including broadening participant diversity and making trials more patient-centric.

This collection of in-depth articles comes handpicked from the pages of Research Practitioner, CenterWatch’s trusted bimonthly professional development journal.

Best Practices for Clinical Trial Site Management will help take clinical trials — and one’s career — to a new level of success, explaining:

  • Eight principles of data quality
  • Which documents regulatory inspectors want to see — and how to make sure they’re readily accessible
  • Statistical tools and methods for conducting root cause analysis
  • FDA guidance on patient-focused trials
  • Common reasons participants drop out of a trial
  • Which kinds of training trial staff needs to handle new technologies
  • Four essential elements of an emergency plan

Successfully coordinate all aspects of = day-to-day site management responsibilities with Best Practices for Clinical Trial Site Management.

Management Report Details:
Best Practices for Clinical Trial Site Management
CenterWatch Management Report

PDF Price:

Easy Ways to Register:
By phone: 888.838.5578 or 703.538.7600

About CenterWatch:
Founded in 1994, CenterWatch is a trusted source and global destination for clinical trials information for both professionals and patients. CenterWatch provides proprietary data and information analysis on clinical trials through a variety of newsletters, books, databases, and information services used by pharmaceutical and biotechnology companies, CROs, SMOs, and investigative sites involved in the management and conduct of clinical trials. As a pioneer in publishing clinical trials information, CenterWatch was the first Internet site to publish detailed information about active clinical trials that could be accessed by patients and their advocates.

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Michelle Butler
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