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Advarra Train the Trainer will take place virtually in August 2022.  This course is designed to help trainers develop software training curricula and hone their training delivery skills. The course will also provide you with a chance to collaborate with other members of the Onsemble community to discuss training successes and challenges. Train the Trainer is a course about how to deliver training for Advarra technology solutions. The Advarra Technology Training Team will guide learners through best practices for curriculum development and training delivery. The course is not specific to one Advarra technology and open to anyone at Advarra’s technology solution customers. There is no formal amount of time required as a trainer to be in this course. Class Schedule: Web session 1: August 8 10-1 CT Web session 2: August 10 10-1 CT Web session 3: August 15 10-1 CT Web session 4: August 17 10-1 CT Capstone Presentations: August 19   Read More

The COVID-19 pandemic has created unprecedented challenges for research sites and institutions, as well as investigators and staff. Clinical trials have been significantly impacted by re-prioritization of resources, staff furloughs and reassignments, and new policies and procedures. The thought of where to begin when research can resume can be overwhelming.  The Advarra team wants to help by providing tools to bring clarity during this chaotic time.  We have created this eLearning module to help you navigate the key considerations around when to restart your clinical research, how to ensure that new policies and procedures are followed, and which studies to reactivate, first.  This eLearning module highlights a variety of important questions that will help you begin your evaluation process. We also provide a downloadable worksheet to help you track your organizational readiness to restart research.  This module has been approved for 1 CEU by the California Board of Registered Nurses (CBRN).  The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 1 hours of CE credit.  Read More

This course covers the guidelines for assessing the safety and well-being of study participants set in accordance with Good Clinical Practice (GCP). Attendance at this program has been approved for 0.50 contact hours of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations. The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 0.50 hours of CE credit. Read More

During a clinical trial, the sponsor will sometimes send a representative known as a monitor to your site to review the study’s progress. This course will discuss how to plan and conduct those monitoring visits.  Attendance at this program has been approved for 0.50 contact hours of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations. The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 0.50 hours of CE credit. Read More

This course covers the initial steps required to identify and begin a clinical trial. You will also learn the fundamentals of protocol feasibility, handling staff and service providers, managing a draft budget and contract, and how to handle IRB submissions. Attendance at this program has been approved for 0.50 contact hours of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations. The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 0.50 hours of CE credit. Read More

The goal of the research is to identify treatments or interventions that can be used on people across age, ethnicity, gender, and lifestyles. If the clinical trial does not represent the population that will ultimately benefit from the study findings, then we won’t have an accurate picture of the efficacy and safety of these treatments in the real world.  However, it is a known issue that many clinical trial populations do not represent the population that will ultimately benefit from the study treatments or interventions. This course will cover the ethical considerations of diversity and inclusion in clinical trials, identify barriers to diversity in research, share practical examples of what diversity in trials could look like and how to increase diverse participation, as well as how to track the effectiveness of your D&I initiatives. Attendance at this program has been approved for 0.50 contact hours of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations. The Society of Clinical Research Associates (SOCRA - www.SOCRA.org) accepts documentation of candidate participation in continuing education programs for recertification if the program is applicable to clinical research regulations, operations or management, or to the candidate’s clinical research therapeutic area. This program offers 0.50 hours of CE credit. Read More

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