MATTER Workshop: The Role of IRB in Research

MATTER members and partners: use your discount code for 100% off the registration price. If you don't know your code, please email info@matter.health for assistance.

ABOUT THIS WORKSHOP

When performing research on humans, there are many regulations that must be followed. Whether collecting data, publishing data, or conducting a research trial, all human-based “research projects” are overseen by the same regulations and governing body.

Join this workshop to understand

• What is and what is not considered a research project.
• The regulations, guidelines and best practices that must be followed.
  
• The research process, from writing a protocol or informed consent to IRB review.

Can't attend in person? Join us in our virtual classroom. To join this workshop virtually via Webex, select the "Virtual classroom" ticket type at checkout - access instructions will be included in your email receipt.

ABOUT THE INSTRUCTOR

Sarah Atwood has over 20 years of experience in Operations and Business Development in Clinical Research. Prior to joining IntegReview in 2014, Sarah was the Vice President for MetaClin Research. She was responsible for the clinical operations of their multiple Phase I – IV clinical research sites and developing the CRO business to provide project management and monitoring services. Prior to management, Sarah has held various positions including Clinical Research Coordinator, CRA, Project Manager and Consultant for CROs and Sponsors and has a background in hospital research, pharma, medical devices, nutraceuticals and biotech. She is a member of Women in BIO and ACRP (Association of Clinical Research Professionals).