CRC Advanced
This course provides clinical research professionals with advanced training tailored to the CRC’s critical role in the conduct of clinical trials.
About this Course
The CRC Advanced course provides clinical research professionals with advanced training tailored to the CRC’s critical role in the conduct of clinical trials. It is designed for CRCs who have taken CRC Foundations, or those with two or more years of experience as a CRC. It complements the foundational course, and may be used for professional development and/or as a refresher course.
Language Availability: English
Suggested Audiences: Clinical Research Coordinators, Clinical Research Professionals, Investigators
Organizational Subscription Price: $500 per year/per site; $800 per year/site (total fee for subscribing to both CRC Foundations and CRC Advanced)
Independent Learner Price: $165 per person; $300 per person for combined option (CRC Foundations and CRC Advanced)
CE Credits and Units
To purchase CE credits and units, you need to be affiliated with an organization that subscribes to this course or buy it as an independent learner first.
Physicians
AMA PRA Category 1 Credit ™
2 credits
(4 CE certified modules)
$40
17 February 2019
16 February 2022
Psychologists
CE Credit/Hour
2 credits
(4 CE certified modules)
$40
17 February 2019
16 February 2022
Other Participants
Certificate of Participation
2 credits
(4 CE certified modules)
$30
17 February 2019
16 February 2022
Course Content
Project Management for Clinical Trials 
Provides an overview of project management principles, how the principles can be applied to managing clinical trials, and how using project management methodologies can increase trial efficiency by minimizing omissions and redundant activities. This module also discusses tools that CRCs can use to help manage a clinical trial.
Recommended Use: Required
ID (Language): 17864 (English)
Author(s): Jessica Derr, BA, CCRC, CRCP - Texas Health Resources; Susan Leister, BS, MBA, PhD, CQA, CSSBB - Technical Resources International, Inc. and University of Phoenix
Preventing and Identifying Misconduct and Noncompliance
Describes the CRC’s role in preventing and identifying misconduct and noncompliance in clinical research, and provides strategies for investigating issues, performing a root cause analysis, and creating a corrective action plan.
Recommended Use: Required
ID (Language): 17865 (English)
Author(s): Nancy Wintering, MSW, LCSW, CCRP - Thomas Jefferson University
Training and Mentoring
Presents practical strategies for experienced CRCs to orient new CRCs, including development of standardized orientation programs that cover essential domains. Discusses continued training and professional development for experienced CRCs, such as mentoring and self-directed learning.
Recommended Use: Required
ID (Language): 17866 (English)
Author(s): R. Jennifer Cavalieri, BSN, RN, CCRC - University of Nebraska Medical Center; Mark E. Rupp, MD - University of Nebraska Medical Center
Financial Management of Clinical Trials
Provides an overview of budget formulation and cost identification, discusses subject remuneration and reimbursement, reviews complex billing issues (including Medicare), identifies how to avoid fraud and abuse in billing, and concludes with the importance of budget reconciliation.
Recommended Use: Required
ID (Language): 17867 (English)
Author(s): Susan Leister, BS, MBA, PhD, CQA, CSSBB - Technical Resources International, Inc. and University of Phoenix
Subject Recruitment and Retention
Identifies regulatory considerations associated with subject recruitment. Discusses the steps in developing a subject recruitment plan, strategies for approaching subjects, barriers to study participation, and challenges and strategies for subject retention.
Recommended Use: Required
ID (Language): 17868 (English)
Author(s): R. Jennifer Cavalieri, BSN, RN, CCRC - University of Nebraska Medical Center; Mark E. Rupp, MD - University of Nebraska Medical Center
Statistics and Data Management of Clinical Trials
Describes the role of statistics and informatics in research, including an overview of different study designs and the application of biostatistics to determine sample size. The module also discusses clinical data management and the significance of data quality.
Recommended Use: Required
ID (Language): 17869 (English)
Author(s): Farida Dabouz, PhD, CCRP
Specialty Areas and Regulatory Requirements
Provides a brief overview of several specialty areas and regulations that CRCs may encounter in the conduct of clinical research with investigational products, including: electronic records, systems, and signatures; research with biologics; good manufacturing practice (GMP); and shipping and receiving hazardous and dangerous goods.
Recommended Use: Required
ID (Language): 17870 (English)
Author(s): Nancy Wintering, MSW, LCSW, CCRP - Thomas Jefferson University