Danielle has a background in life sciences, with over 15 years of cumulative healthcare and clinical research experience specializing in the management and regulatory oversight of domestic and global clinical trials in multiple therapeutic areas.  She has advanced knowledge of federal regulations, ICH GCP guidelines and ethical codes governing the protection of human subjects.  Danielle has also served as a clinical assessor and mentor for new CRAs. She has also helped to audit clinical research training modules and assessments for new CRAs. Danielle's experience along with her commitment to industry diversification led her to begin coaching other professionals interested in career development or career change on how to enter clinical research.