Jessica is a highly accomplished and dedicated professional with over 20 years of experience as Director Site Management within the Contract Research Organization (CRO) industry. With her extensive knowledge of clinical trial management, regulatory compliance, and operational efficiency, she has consistently led cross-functional teams to successfully execute numerous clinical trials and studies. Her warm and approachable nature fosters a harmonious work atmosphere that encourages open communication and teamwork.

In her current role as Global Site Activation and Monitoring Head for Benelux , Jessica upholds the highest standards of quality and compliance for the Clinical Operations team in the Benelux region. She consistently seeks opportunities for process improvement and implements innovative strategies to enhance efficiency and mitigate risks in clinical operations. Maintaining close collaboration with local sponsor affiliates, she drives project success through effective communication and partnerships.

Jessica’s journey in Clinical Research began in March 2004 and she has held various critical positions including Clinical Trials Assistant, Clinical Research Associate, Dedicated Trip Report Reviewer, RSU Team Lead, Clinical Operations Manager and Associate Director. Throughout her career, she has been responsible for the full lifecycle of clinical trials, from start-up (feasibilities & site-ID) to project close-out and review.

With extensive expertise spanning full range of therapeutic indications and Medical devices, Jessica has demonstrated her ability to handle diverse clinical research areas with excellence.

Moreover, Jessica actively participates in global initiatives, including strategic site relationships, early talent training programs, CRA training improvements, and risk-based monitoring roll-out models. Her commitment to professional development and industry advancements is evident through her leadership in the Site Management Line Manager forums.