Past CCCR Webinars

Title: AHS Navigating Health System Access Resources

Date: Wednesday January 24th , 2024

Presenters:

  • Noopur Swadas, RN BN, Advisor  |  Health System Access  |  Health Evidence & Innovation | Alberta Health Services
  • Leanne Blahut

Objectives:

  • Understand the HSA Administrative Approval Process: From Start to Finish
  • Explore Tools and Resources for Health Research via the Provincial Health System. SharePoint Platform within the Provincial Health System.

To view slide deck please see here

____________________________________________

Title: OnCore Financials Deep Dive

Date: Wednesday March 20th , 2024

Presenters:

  • Mari Boesen, MSc PMP, CTMS Provincial Project Manager

Objectives:

  • Understand the different charge types in OnCore and how to trigger them
  • Be able to locate invoiceable items in OnCore
  • Appreciate the differences between invoices from OnCore and invoices from PeopleSoft

To view slide deck please see here

____________________________________________

Title: AHS Biosafety for Research and Clinical Trials Policy

Date: Wednesday April 24th , 2024

Presenters:

  • Joseph Roberts, Alberta Health Services Provincial Lead – Research Integration

Objectives:

  • AHS has recently adopted a new Biosafety for Research and Clinical Trials policy. How research and clinical trials are reviewed and approved by AHS remains the same.
  • This webinar discusses how the policy strengthens AHS’ ability to support Principal investigators using advanced interventions by:
  • Complying with the federal Human Pathogens and Toxins Act and Regulations
  • Applying a consistent approach to assess and manage biosafety and biosecurity risks, and
  • Enabling trials whose sponsors require established procedures for biosafety review.

To view slide deck please see here

____________________________________________

Title: Electronic signatures in Adobe Sign & 21 CFR Part 11 Compliance

Date: Monday May 6th , 2024

Presenters:

  • Jenna Dobry, Lead Regulatory Officer

Objectives:

  • When to use Adobe Sign for electronic signatures in clinical research
  • What are the 21 CFR Part 11 requirements
  • How Adobe Sign meets these requirements with the new Bio-Pharma settings
  • How the new settings have impacted sending a document for signature
  • How the new settings have impacted signing a document

To view slide deck please see here

____________________________________________

Title: CSM Legal: IRISS Contract Module Adoption

Date: Monday October 7th, 2024

Presenters:

  • Stephen Harris, Director and Senior Legal Counsel
  • Manjari Shukla, Senior Contract Administrator

Objectives:

  • Understand the reasons for transitioning to IRISS and its enhanced functionalities.
  • Understand CSM Legal's agreement classifications and their purpose.
  • Learn about common IRISS submission errors and how to avoid them.

To view slide deck please see here

To view recorded webinar please see here

____________________________________________

Title: Researcher's Guide to Clinical Trials at the University of Calgary

Date: Monday November 4, 2024

Presenter:

  • Mari Boesen, MSc PMP, Provincial Project Manager, OnCore CTMS

Objectives:

  • Know where to access the new Researcher's Guide to Clinical Trials at the University of Calgary
  • Be able to explain the purpose and scope of the new guide
  • Have a general understanding of the systems, teams, and processes for clinical trial workflows at the UC

To view slide deck please see here

To view recorded webinar please see here

____________________________________________

To view Past Lunch and learn Webinars and slide decks please click here

____________________________________________

Title: HOW TO …Save Time by Using OnCore System Integrations

Date: Monday January 30th, 2023

Presenter: Mari Boesen, Provincial CTMS Project Manager and Gillian Hughes, CTMS Implementation and Training Lead

Objectives:

  • Become familiar with the existing IRISS, PeopleSoft, and Connect Care integrations
  • Understand how CTMS integrations save time in research administration
  • Learn about future integrations with OnCore

To view slide deck please see here

______________________________________________

Title: What's New at the Calgary Centre for Clinical Research

Date: Monday March 27th, 2023

Presenters:

  • Gillian Hughes, Manager, Clinical Trial System Services, Provincial OnCore Support Team (POST)
  • Asim Nadeem, Clinical Research Finance Lead
  • Jenna Dobry, Quality Assurance and Regulatory Compliance Specialist

Objectives:

  • The OnCore Clinical Trial Management System is becoming mandatory – find out what this means
  • CCCR is taking over clinical trial invoicing – hear what is changing
  • CCCR is offering monitoring – learn more about this new service

To view slide deck please see here

______________________________________________

Title: AHS Health System Access @ U of C

Date: Monday June 19th, 2023

Presenters:

  • Noopur Swadas, RN BN, Advisor  |  Health System Access  |  Health Evidence & Innovation | Alberta Health Services

Objectives:

  • Meet the HSA team
  • Understand the role and function of HSA
  • Learn tips to expediate your AHS administrative approval and ask questions!

To view slide deck please see here
______________________________________________

Title: Research in Connect Care Webinar

Date: Wednesday September 20th, 2023

Presenters:

  • Wendy Pratch | Registered Nurse | Clinical Informatics Lead (CIL) 

Objectives:

  • Study in-take process (will emphasize the importance of responding to communications, etc.)
  • Roles and Access
  • Training Sequencing and Requirements
  • Research Conversion
  • Importance of the research icon

To view slide deck please see here

______________________________________________

HOW TO...Use The OnCore Clinical Trial Management System CTMS

Dec 12th, 2022

Speaker:  Mari Boesen, Provincial CTMS Project Manager and Gillian Hughes, CTMS Implementation and Training Lead

Objectives:

  • Understand how a CTMS facilitates study administration 
  • Learn about the core CTMS functionality  and integrations
  • Become familiar with the OnCore Happy Path

>>View Slide Deck  

______________________________________________

HOW TO... Meet Research Data Management Requirements With The Help of The CRU

Nov 28th, 2022

Speaker: Chelsea Wellman, and Jesse Hart Szostakiwsky

Objectives:

  • Outline the basic requirements detailed in the Tri-Agency Council's Research Data Management Policy.
  • Discuss how the Clinical Research Unit (CRU) can support researchers to meet these requirements.

>>View Slide Deck  

______________________________________________

HOW TO... Navigate CSM Legal for your Clinical and Non-Clinical Research Agreements

Oct 24th, 2022

Speaker: Sarah Menzies, Legal Counsel - Legal and Research services, CSM Legal

Objectives:

  • New changes and improvements to the CSM Legal department
  • Who is on the CSM Legal team and what do they do?
  • Tips for researchers to facilitate faster agreement turn-around-times

>>View Slide Deck  

______________________________________________

HOW TO... Utilize the AHS Research Pharmacy For Your Clinical Research

Sep 26th, 2022

Speaker: Candice Cameron BA, BSP, ACPR, Pharmacist, Pharmacy Research Service, Alberta Health Services – Calgary Zone

Objectives:

  •   To learn what services the AHS Research Pharmacy offers
  •  To learn how and when to engage the AHS Research Pharmacy

>>View Slide Deck       

______________________________________________

HOW TO... Recruit for your Research Study

Speaker: Joslyn Gray, Project Manager, ACHIEVE Research

Objectives:

  • will introduce effective ways to promote your research study 
  • demonstrate different strategies for recruiting into a research study 
  • produce examples of ways to increase participant retention 

>>View Slide Deck        >>View Webinar 

______________________________________________

HOW TO …do remote consenting -  Introducing the NEW REDCap eConsent Tool

May 30, 2022

Speaker:  Chelsea Wellman, CRU Senior Project Coordinator.

Objectives:

  • To provide an overview of eConsenting, its benefits and regulatory requirements
  • To demo the NEW REDCap eConsent Tool
  • To provide details on how to access the REDCap eConsent Tool

>>View Slide Deck     >>View Webinar

______________________________________________

HOW-TO… Navigate the New IRISS AHS Module 

April 25, 2022

The new AHS application module is now integrated directly within IRISS and replaces the previous SharePoint form. 

The application is built on SmartForm logic and pulls information directly from the ethics application to guide study-specific.

Presenters:

Stacey Beck - Senior Consultant, Systems Dev, Office of Research Services, University of Calgary 
Becky Wong – Director, Health System Access, Alberta Health Services 

Key Features:

  • visibility into the current state of your application 
  • ability to save, edit, and continue the application at any point 
  • automatic data sync with REB and AHS records so information is always current 
  • communicate directly with the AHS team through IRISS 

>> ASH Module - User Guide 

______________________________________________

Demystifying Decentralized Trials -  IQVIA’s Patient-Centric Decentralized Clinical Trial Solutions

February 28, 2022

This session was about Demystifying Decentralized Trials - IQVIA’s Patient-Centric Decentralized Clinical Trial Solution.

Presenter: Sylvie Cornibert, Strategic Site Solutions Manager, Strategic Site Solutions, US and Canada, IQVIA R & DS Operations

Learning objectives:

  • Decentralized/Virtual Trials, where is it going?
  • What does it look like now and likely to look like for the foreseeable future.
  • Presentation of the IQVIA technology for Decentralized Trials What is the impact of Decentralized/Virtual Trials in general on site research staff?

>>View Slide Deck     >>View Webinar

______________________________________________

"If we are all in this together, why do I feel *insert feeling here*?"

January 24, 2022

This session focused on mental health, wellbeing and discussions regarding examples and resources for you and your team. We understand that you and your team may be feeling *overwhelmed, guilty, unmotivated, resentful…* and we are here to discuss how to manage those feelings within yourself and your team. *This session was not recorded *

Facilitators:

  • Michele Moon, MSc BScOT (she/her), Team Lead, WellBeing and WorkLife, Staff Wellness
  • Amanda Habiak, RN, BN, OHN (she/her) Consultant, Mental Health, Staff Wellness

Learning Objectives:

  • To recognize and identify the impact of the current circumstances and stressors on our selves, team and work.
  • To explore a new and improved conceptualization of resilience.
  • Find and use resources to help ourselves and others within our team.

>> View Slide Deck

______________________________________________

Health Research Platform Lunch & Learn, Nov 22, 2021

Title:  Moral Distress, Compassion Fatigue and Burnout within your Research Team

Presenter:  Daniel Garros, Clinical Professor, Dept. of Pediatrics, Div of Critical Care, University of Alberta, Stollery Children’s Hospital PICU

Learning Objectives:

  • Describe old concepts: Moral Distress and Compassion Fatigue
  • Explore new Concepts: Moral injury and Moral Hazard
  • Apply the research results on Moral Distress into practice: how to resolve it
  • How such ideas would help me solve nmy “angst” doing research in the present healthcare climate

>> View Webinar

______________________________________________

Health Research Platform Lunch & Learn, Oct 21, 2021

Title: Whistleblowing and Research Misconduct

Presenters

Shirley Vonya Wilson, Protected Disclosure Advisor, Protected Disclosure and Research and Integrity Office, University of Calgary

Stacey Page, PhD, Chair, Conjoint Health Research Ethics Board, Associate Professor, Department of Community Health Sciences, Cumming School of Medicine, University of Calgary 

Learning Objectives:

  • to appreciate what research and scholarly integrity is and why is is important
  • to understand what things are considered breaches of research and scholarly integrity
  • to be aware of options and avenues to report concerns about research and scholarly integrity

>> View Slide deck

______________________________________________

Health Research Platform Lunch & Learn, Sept 27, 2021

Title: Because ICH Says So

Presenter: Mari Boesen MSc PMP, CTMS Implementation Project Manager, Clinical Research, University of Calgary

Learning Objectives:

  • appreciate the history behind clinical trial regulation
  • explain how ICH came to be
  • understand the importance of regulatory compliance

>> View Webinar 

______________________________________________

Health Research Platform Lunch & Learn, Apr 26 2021

Title: Research Ethics Board Exchange (UA/UC multi site process)

Speakers: 

  • University of Alberta, Kim Kordov, Associate Director Research Ethics
  • University of Calgary, Joan Fennell, Manager, Research Ethics & Compliance

>> View Slide deck

______________________________________________

Health Research Platform Lunch & Learn, Feb 22 2021

Title: Patient Engagement in Health Research

Speakers: 

  • Maria Santana, Provincial Lead & Assistant Professor, Departments of Pediatrics and Community Health Sciences, University of Calgary
  • Paul Fairie, Associate Director
  • Sandra Zelinsky, Lead Patient Research Partner
  • Sumedh Bele, Assistant Director
  • Sadia Ahmed, Research Coordinator
  • Ingrid Nielssen, Patient Engagement Coordinator Lead
  • Tiffany Barbosa, Community Engagement Coordinator

>> View Webinar

______________________________________________

Health Research Platform Lunch & Learn, January 25 2021

Title: The Quality Assurance and Regulatory Compliance Program for Clinical Research: Lessons Learned 

Speaker: Linda Longpré, CCRP, Quality Assurance and Regulatory Compliance Specialist, Calgary Centre for Clinical Research

>> View Webinar 

Health Research Platform Lunch & Learn, November 30 2020

Title: Shared Investigator Platform Initiative at U of C

Speakers:

  • Shweta Patel, Clinical Trial Program Administrator, Calgary Centre for Clinical Research (CCCR), University of Calgary 
  • Delaine Ramesh, SIP Implementation Strategy Lead CCO Canada, Hoffmann-La Roche Limited
  • Suzan O'Donnell, Country Specialist/Shared Investigator Platform (SIP) Country Point Person, Hoffmann-La Roche Limited  

>> View Webinar 

______________________________________________

Health Research Platform Strategy Lunch & Learn, October 26 2020

Title: A Clinical Trial Management System for the U of C - A Game Changer in the Conduct of Clinical Trials

Speaker: Sabine Moritz, Director, Clinical, Health Services and Population Health Research

>> View Webinar 

______________________________________________

Health Research Platform Strategy Lunch & Learn, September 28, 2020

Title: Running a Virtual Study: Lessons Learned from the Alberta HOPE COVID-19 Clinical Trial

Speakers:

  • Mari Boesen, Associate Director, Pragmatic Clinical Trials Platform, Alberta SPOR SUPPORT Unit, University of Calgary
  • Elizabeth Baguley, Research Administrative Assistant, Liver Unit, University of Calgary

>> View Webinar 

______________________________________________


Have questions or comments?

Inquiries regarding education and training opportunities should be directed to Becca McInnes

Becca McInnes

cccr@ucalgary.ca