innovations during the drug
discovery phase.
We take a personalized and integrated approach to help our clients position their pipelines and companies for success offering a full range of development and commercialization services.
We are Halloran, a life science consulting firm, partnering to enrich your product development and business growth. We propel your organization further; positively impacting the health and wellbeing of patients around the world.
Elizabeth Bodi has over 32 years of experience in the biopharmaceutical and medical device industries. Liz has expertise in quality and compliance with a primary focus on clinical operations and clinical quality assurance activities to ensure excellence and compliance across phase I-V clinical trials. Specific experience in the management of clinical quality assurance programs including site, vendor, and process audits. Additionally, skilled in the implementation of quality system initiatives – such as developing SOPs, conducting gap analyses and remediation, establishing and/or managing quality groups, conducting inspection readiness activities including behavioral coaching and mock inspection, hosting regulatory authority inspections, and the development and delivery of training courses in clinical research management and GCP.
Before joining Halloran, Elizabeth worked in the Clinical Training and Compliance group at Antigenics where she was responsible for the development and implementation of Clinical Trial Management Systems (CTMS), quality assurance, and standard operating procedures. Elizabeth has held roles as a Clinical Research Associate (CRA) at Covance, and Training Manager at PAREXEL International, and MTRA/AAI.
Boston University, Bachelor of Science in Cardiopulmonary Sciences
Boston University, Master of Science in Applied Anatomy and Physiology
RQAP-GCP Certified