With the current/recent global pandemic, many clinical trial sites had to adopt technology and adapt processes to allow remote work. This webinar continues our dive into decentralized clinical trials (DCTs) and their impact on clinical sites. The webinar explores how the increased use of technology is impacting the workforce.
During this review, we will discuss the implications of DCTs on traditional clinical research positions and what new roles will likely be needed. This webinar identifies new skills site staff will need to be successful when working in this new research environment.
Note: It is recommended that learners should complete the webinar Understanding Decentralized Clinical Trials (DCTs) and Virtual Study Visits prior to this webinar.
Language Availability: English
Suggested Audiences: Sites, Graduate Students, Clinical Research Coordinators, Researchers, Students
Organizational Subscription Price: $300 per year/per site or included as part of the $1,000 annual subscription to our All Access Webinar Package
Independent Learner Price: $49 per person
Decentralized Clinical Trials (DCTs) and Your Workforce
Presented by: Kimberly Ray, BS - Clinical Reseach Consultant
- Describe some technology solutions typically used in decentralized clinical trials (DCTs).
- Explore how traditional clinical research jobs at investigational sites are changing when conducting DCTs or trials that use many types of technology.
- Identify any new skills that are necessary to conduct clinical research in this new environment.
- Explore new positions and roles that may be needed for DCTs.
Recommended Use: Required
ID (Language): 20432 (English)
Understanding Decentralized Clinical Trials (DCTs) and Virtual Study Visits
Introduces DCT models and components, and provides best practices for virtual study visits.
Remote Informed Consent: The Same, but Different, but Still the Same
Presents remote consent considerations and scenarios.
Good Clinical Practice (GCP)
Provides essential GCP training for research teams involved in clinical trials of drugs, biologics, devices, and behavioral intervention and social science studies.
Provides clinical research professionals with basic and advanced training tailored to the CRC’s critical role in the conduct of clinical trials.
This course provides information on basic techniques for data and device security, including email and mobile devices.
Research Study Design
This course provides learners with an understanding of how to improve study design, collect and analyze data, and promote reproducible research.
Technology, Ethics, and Regulations
Covers various technologies and their associated ethical issues and governance approaches.