Upcoming Webinar

Adapting to the Evolving Era of Oncology: Implications and Strategies for Research Institutions

Oncology research is entering a transformative phase, with breakthroughs in biomarker-directed therapies and innovations that are reshaping the treatment landscape. As research institutions navigate this "Golden Era," ensuring ethical rigor, regulatory compliance, and robust protocol design has never been more critical.

How prepared is your institution to navigate the intricacies of oncology research involving complex genomic data in today’s evolving landscape?

Join Vanessa Hill, Director Research Compliance, Advarra and Michelle Green, Genomics Program Manager, LabCorp for an insightful discussion on the latest ethical and regulatory challenges for research institutions in oncology research.

Learning Objectives:

  • Navigate complex ethical considerations in oncology studies
  • Implement best practices to ensure adherence to evolving regulatory frameworks
  • Proactive approaches for addressing unique challenges in oncology trials, including patient safety and data integrity

Presented By

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Michelle Green

Genomics Program Manager
LabCorp Oncology

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Vanesa Hill

Director, Research Compliance, Institutional Research
Advarra

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Assistant Clinical Professor, Internal Medicine and Pediatrics
Conventus Site Medical Director for UBMD

Adult Transitional Sickle Cell Program Director Department of Medicine
Jacobs School of Medicine and Biomedical Sciences University of Buffalo

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Who should watch?

This content applies to VPs of Research, Institutional Officials, IRB/HRPP professionals, research compliance professionals, research professionals from research institutions, academic medical centers, hospital systems, and other sites with local IRBs, research professionals planning and conducting multisite clinical trials, and others involved in IRB/HRPP activities for multisite clinical trials. Research professionals from research institutions, academic medical centers, hospital systems, and other sites with local IRBs, IRB professionals, research professionals planning and conducting multisite clinical trials regulated by FDA, and others involved in IRB activities for multisite clinical trials.

CE Credits

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.

This event may qualify for continuing education (CE) credits. Please check with your professional organization(s) to determine whether the event meets their CE eligibility 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.

DATE: October 24, 2024
TIME: 1:00 pm ET | 10:00 am PT
DURATION: 1 hour

Register Now