FALLS CHURCH, Va., March 12, 2019 /PRNewswire-PRWeb/ -- Data Integrity in Clinical Trials **A CenterWatch Webinar** Tuesday, March 26, 2019, 1:30 p.m. - 3:00 p.m. EDT
https://store.centerwatch.com/p-584-data-integrity-in-clinical-trials.aspx
In this competitive and pressured filled world, even seasoned professionals may take shortcuts, engage in inappropriate behavior or fail to disclose errors or problems in data.
Data integrity problems occur within an institutional culture.
Donna Kessler, PhD., Research Integrity Officer at Duke University, will discuss the increased focus — nationally and globally — on the reliability of research data, honesty in reporting, and data reproducibility in an era of heightened competition and pressure. Over the course of 90-minutes she'll help attendees understand:
Meet Your Presenter: Donna Kessler, PhD., Research Integrity Officer, Duke University
Dr. Kessler is the misconduct review officer at Duke and oversees the investigation of potential research misconduct. She also participates in Responsible Conduct of Research (RCR) education at Duke and presents nationally on RCR and research integrity. Dr. Kessler conducted research and taught classes in the physical and life sciences, and has prior experience in research administration as a funding officer/program manager, managing intellectual property assets at NC State and Duke, and as a Chair on the Duke IRB.
Who Will Benefit
Tuition: $287 per site
Easy Ways to Register: Online: https://store.centerwatch.com/p-584-data-integrity-in-clinical-trials.aspx By phone: 617-948-5100 or 866-219-3440
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.
SOURCE CenterWatch
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Data integrity problems occur within an institutional culture.
Donna Kessler, PhD., Research Integrity Officer at Duke University, will discuss the increased focus — nationally and globally — on the reliability of research data, honesty in reporting, and data reproducibility in an era of heightened competition and pressure. Over the course of 90-minutes she'll help attendees understand:
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- How regulatory authorities are defining research misconduct, and how to avoid legal hot water by complying with clinical research integrity guidelines in consent forms and marketing disclosures
- What are questionable research practices (QRPs), especially in dealing with vulnerable populations
- How to avoid wrongdoing in your clinical research by complying with current regulatory guidelines for proper conduct
- How costly wrongdoings are in clinical research on both the personal and professional level
- Tips for compliance in conducting proper research in the areas of subject recruitment, consent, record-keeping, and patient outreach and communication
Meet Your Presenter: Donna Kessler, PhD., Research Integrity Officer, Duke University
Dr. Kessler is the misconduct review officer at Duke and oversees the investigation of potential research misconduct. She also participates in Responsible Conduct of Research (RCR) education at Duke and presents nationally on RCR and research integrity. Dr. Kessler conducted research and taught classes in the physical and life sciences, and has prior experience in research administration as a funding officer/program manager, managing intellectual property assets at NC State and Duke, and as a Chair on the Duke IRB.
Who Will Benefit
- Clinical Quality Assurance Professionals
- Clinical Operations Professionals
- Data Management Professionals
- Clinical Trial Electronic Systems Developers
- Clinical Trial Statisticians and Statistical Programmers
- Clinical Investigators and Clinical Investigator Site Staff
- Regulators- GCP Inspectors
- Regulators- Reviewers/Assessors of Clinical Trial Data
Tuition: $287 per site
Easy Ways to Register: Online: https://store.centerwatch.com/p-584-data-integrity-in-clinical-trials.aspx By phone: 617-948-5100 or 866-219-3440
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.
SOURCE CenterWatch
