Kathleen Squillace is Vice President Global Clinical Operations at Veeda Oncology. Ms. Squillace has over 30 years of research experience including 20 years in oncology. Initially, Ms. Squillace developed animal models at the National Institutes of Health and later moved into the clinical arena. She worked in the oncology group at Adria (Pharmacia) and assisted in several New Drug Application (NDA) submissions. Ms. Squillace was the project planner for a Cooperative Research and Development Agreement (CRADA) with the NCI which included approximately 35 Phase I and Phase II studies. For over 10 years, she worked as an independent consultant providing a wide range of oncology-focused services to such companies as Battelle Memorial Institute, Pharmacia and Upjohn, IDEC Pharmaceuticals, Neoprobe, and the Ohio State University.

Having worked as a Project Manager, Clinical Research Manager, Quality Assurance Auditor, Medical Writer and Senior Clinical Research Associate, Ms. Squillace has expertise in the planning and execution of clinical trials including protocol design, budget and timeline preparation, study initiation activities, CRF development, AE/SAE review and reporting, QA auditing, protocol and final study report writing and resource management. Ms. Squillace most recently was Senior Director of Clinical and Project Management at Prologue Research, an oncology CRO. In that role, she was responsible for Project Management, Clinical Projects, Medical Writing, Monitoring Services and Pharmacovigilance.

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