Sponsors and CROs involved in working with research sites share in the responsibility to ensure that investigators and research staff are appropriately qualified to protect subjects in research and know how to comply with IRB regulatory requirements. That’s why clinical research associates working on behalf of sponsors and CROs must also possess sufficient knowledge of IRB requirements and principles in human subject protection to serve as an effective resource to sites. Because insufficiently trained CRAs can affect a site’s ability to comply with IRB requirements, HRP offers the following training opportunities for CRAs:
- Distinguishing unanticipated problems from serious adverse events.
- Reporting unanticipated problems and non-compliance.
- Protecting subject privacy and confidentiality.
- Proper recruitment methods.
- Fulfilling IRB consent requirements.
- Achieving efficient IRB approval.
- Record-keeping and case report form completion.
We are always looking for ways to deliver our services in ways that are both convenient and cost-effective. We are pleased to offer you webinars for any of our education and training services. To learn more about our webinars or to request a webinar on a particular topic, please contact us at (347) 862-9321 or by email at services@thehrpconsultinggroup.com.