FALLS CHURCH, Va., Sept. 29, 2020 /PRNewswire-PRWeb/ -- The CRC
Trainer
An Interactive Companion to the CRC's Guide to Coordinating
Clinical Research
CenterWatch eLearning
https://www.centerwatch.com/products/472-the-crc-trainer
Wherever one falls on the spectrum of clinical research
management, The CRC Trainer: An Interactive Companion to the CRC's
Guide to Coordinating Clinical Research provides the perfect
interactive course to support learning the skills necessary for the
role. Since book learning doesn't work for all, it's nice to have a
self-paced, interactive option to evaluate how well one retains
information.
The CRC's Guide to Coordinating Clinical Research has long been
looked at as the preeminent resource for training new CRCs and
keeping experienced coordinators up-to-date on relevant changes in
regulations. The detailed information in the guide covers
everything a coordinator needs to know to succeed in the role — and
The CRC Trainer: An Interactive Companion to the CRC's Guide to
Coordinating Clinical Research makes digesting that information
simpler and straightforward.
This visual, interactive eLearning course was built to support
learners in a self-paced journey through the complex material of
the guide. It covers all essential aspects of the CRC role and
focuses learners on the most important aspects of the guide.
During this eLearning course, we will cover:
- The role and responsibilities of CRCs
a. Qualities in an effective CRC
b. Regulatory history and shifting
rules
- The clinical research process
a. Trial site quality systems
b. Writing SOPs
c. Research: from lab to trial to
closeout
- Study preparation, protocols and reporting
a. Site qualifications
b. Working with vulnerable populations
c. Ensuring data quality
- Trial participants, closures, monitoring and inspections
a. Working with sponsors and
monitors
b. Storage of trial materials
c. Working with IRBs and data safety
monitoring boards
d. Principles and challenges of informed
consent
e. Adverse event and safety monitoring
f. Quality management and audits
The six modules of the course can be uploaded to a PC for use by
individual trainees or added to an organization's learning
management system (LMS) to track and evaluate the progress of
multiple trainees. A certificate of completion is awarded to
trainees who pass the final exam.
This indispensable tool provides the skills and knowledge that
are critical for managing clinical trials. Join other clinical
trial professionals on the path to effective management.
Attendance at this program has been approved for a total of 3.00
contact hour of research specific continuing education on
applications for Maintenance of ACRP's CCRC®, CCRA®, CPI®, or
ACRP-CP® certification designations.
Webinar Details:
The CRC Trainer:
An Interactive Companion to the CRC's Guide to Coordinating
Clinical Research
CenterWatch eLearning
https://www.centerwatch.com/products/472-the-crc-traine
eLearning Package:
Single User - $295
Multi-user buyers and licenses:
- 2-10 users – $275 per user
- 11-20 users – $255 per user
- 21-30 users – $235 per user
- 31-40 users – $215 per user
- 41-50 users – $200 per user
- 50+ users – Contact Bailey
Sterrett at +1 703.538.7637 for LMS licensing prices.
Easy Ways to Register:
Online:
https://www.centerwatch.com/products/472-the-crc-trainer
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.
SOURCE CenterWatch