Danielle is an experienced clinical research coordinator and site manager with over 5 years of experience supporting the successful execution of clinical trials across a wide range of therapeutic areas. Throughout her career, Danielle has demonstrated a strong commitment to operational excellence, regulatory compliance, and the advancement of high-quality clinical research.

Danielle has extensive experience managing all phases of clinical trials, including study start-up, patient recruitment and retention, protocol implementation, data collection, and close-out activities. Danielle is well-versed in Good Clinical Practice (GCP) guidelines and have a proven track record of maintaining audit-ready documentation and ensuring adherence to study protocols and regulatory requirements.

Known for her collaborative approach, Danielle works effectively with investigators, sponsors, and cross-functional teams to support efficient study execution and positive patient outcomes. Danielle’s ability to manage staffing and complex studies while maintaining attention to detail has contributed to the successful completion of over 75 clinical trials.