Elizabeth Weeks-Rowe

About the Author

Elizabeth Weeks-Rowe is a distinguished expert in clinical research compliance and regulatory affairs, with over two decades of experience guiding organizations through the complexities of monitoring and auditing clinical trials. As a former director of quality assurance at a leading pharmaceutical firm, she has authored numerous resources that demystify the regulatory landscape for professionals in the field. Her practical insights and meticulous attention to detail have made her a trusted voice in ensuring ethical and efficient research practices. In her latest work, The CRA's Guide to Monitoring Clinical Research, Fifth Edition, Weeks-Rowe updates essential strategies for clinical research associates navigating evolving FDA guidelines and global standards, empowering readers to uphold the highest levels of integrity in biomedical innovation.