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This course will be conducted virtually in January, April, July, and October 2024.  Attendees will be asked to participate in several instructor-led web training sessions and complete various pre/post-class activities during the two (2) days. This course utilizes a blend of instructor-led training, eLearnings, independent activities, and other assignments.  Certification candidates must complete a hands-on build project within 30 days of attending the course. OnCore Certification is for users with an intermediate to advanced working knowledge of their institution's workflows. We do not recommend this course for anyone who is not proficient with OnCore. Please see our ILT catalog under Resources for beginner to advanced level courses. Duration: Two (2) days of web-based training activities Date & time: All sessions are Thursday and Friday from 10 am CT - 1 pm CT January 11 - 12 April 4 - 5 July 11 - 12 October 10 - 11 Read more

This course will be conducted virtually in January, April, July, and October 2024.  Attendees will be asked to participate in several instructor-led web training sessions and complete various pre/post-class activities during the two (2) days. This course utilizes a blend of instructor-led training, eLearnings, independent activities, and other assignments.  Certification candidates must complete a hands-on build project within 30 days of attending the course. OnCore Certification is for users with an intermediate to advanced working knowledge of their institution's workflows. We do not recommend this course for anyone who is not proficient with OnCore. Please see our ILT catalog under Resources for beginner to advanced level courses. Duration: Two (2) days of web-based training activities Date & time: All sessions are Thursday and Friday from 10 am CT - 1 pm CT January 11 - 12 April 4 - 5 July 11 - 12 October 10 - 11 Read more

This course will be conducted virtually in March and September 2024.  Attendees will be asked to participate in several instructor-led web training sessions and complete various pre/post-class activities during the four (4) days. This course utilizes a blend of instructor-led training, eLearnings, independent activities, and other assignments.  Certification candidates must pass an exam and complete a hands-on build project within 30 days of attending the course. OnCore Certification is for users with an intermediate to advanced working knowledge of their institution's workflows. We do not recommend this course for anyone who is not proficient with OnCore. Please see our ILT catalog under Resources for beginner to advanced level courses.   Duration: Four (4) days of web-based training activities   Dates & time: Sessions are M-Th from 10 am CT - 1 pm CT March 4 - 7 September 9 - 12 Read more

Medical interventions that are used to treat human illness undergo rigorous development processes in clinical trials before they have been approved for use. A wide variety of items are considered to be healthcare research, such as medical devices, diagnostic tools, behavioral activity, exercises, and nutrition plans. Principal Investigators play a key role in the success of conducting clinical research. This course covers the general phases of clinical trials (focusing on drugs, biologics, and vaccines), defining the difference between clinical research and clinical care, and the responsibilities of a Principal Investigator for ensuring safety and compliance in a clinical trial. 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

Medical interventions that are used to treat human illness undergo rigorous development processes in clinical trials before they have been approved for use. A wide variety of items are considered to be healthcare research, such as medical devices, diagnostic tools, behavioral activity, exercises, and nutrition plans. Clinical Research Coordinators play a key role in the success of conducting clinical research. This course covers the general phases of clinical trials (focusing on drugs, biologics, and vaccines), defining the difference between clinical research and clinical care, and the responsibilities of a Principal Investigator for ensuring safety and compliance in a clinical trial. 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

Human Subjects Protection (HSP) training is essential for investigators and research staff. HSP training describes how investigators, sponsors, and IRBs work together to protect the rights, safety, and well-being of subjects on clinical trials.  HSP training aims to ensure that: the rights, safety, and well-being of human subjects are protected privacy and confidentiality of human subjects in research are maintained View each video to learn more about different topics in HSP.  To pass this course, you must complete the assessment with a score of 80% or greater.  Attendance at this program has been approved for 1.00 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 1.00 hours of CE credit. Read more

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