On-Demand Webinar

The New Normal: Considerations for Restarting Research

Throughout the COVID-19 pandemic, we have continually heard what the “new normal” could mean for our work lives, social lives, schools, communities, and our medical system. But what does it mean for research? What are some of the challenges facing sites, institutions, sponsors and CROs? Research has continued through the crisis, but the environment has changed.

In this webinar, Michele Russell-Einhorn, Joan Versaggi, Wendy Tate, and Judith Carrithers of Advarra will discuss key areas to consider as we look to ramp up research. Topics include required communication with stakeholders both within and external to the research organization, considerations when prioritizing the research portfolio, and process recommendations to ensure compliance and participant and staff safety.

Learning Objectives

Following this free webinar, attendees will be able to:

  • Analyze policies, procedures, and workflows that need review (and potential modification) due to COVID-19
  • Understand how to structure a plan to ensure communication, compliant documentation, and reporting from the shutdown period into the next phase of research conduct
  • Identify specific concerns relating to ongoing and new IRB review of research
  • Provide tools and resources to evolve research workflows, ensuring success in the post-COVID-19 landscape

Presented By

Michele Russell-Einhorn_orange.png

Michele Russell-Einhorn

JD

Chief Compliance Officer and Institutional Official
Advarra

Wendy Tate_dark green.png

Wendy Tate

PhD, GStat

Director, Research Operations
Advarra

Judith Carrithers_blue.png

Judith Carrithers

JD, MPA

Director of Regulatory Affairs
Advarra

Joan Versaggi_purple.png

Joan Versaggi

MBA

VP, Consulting
Advarra

Who Should Watch?

This content applies to research professionals involved in developing, conducting, and overseeing research during COVID-19 pandemic, including representatives from sponsors, CROs, sites, and IRBs.

CEU Credits

Attendance at this session has been approved for 1.00 contact hour of research specific continuing education on applications for Maintenance of ACRP’s CCRC®, CCRA®, CPI®, or ACRP-CP® certification designations and 1 hour of continuing education credit for the Certified IRB Professional (CIP) certification. Provider approved by the California Board of Registered Nursing, Provider Number 16549 for 1 contact hour. 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 hour of CE credit. If you would like to obtain CE credits for a different credential, please check with your professional organization to determine if our webinars meet their continuing education requirements.

Certificate of Attendance

After watching this webinar in its entirety and completing the webinar survey, you will receive a certificate of attendance. This certificate will be emailed to you within one business day of watching the webinar. Please note that if your organization has other staff members who wish to get a certificate of attendance, each person must register, watch the webinar in its entirety, and complete the webinar survey. Visit our Webinar Help page for more information on certificates of attendance.

Duration: 1 hour

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