Speaker Profile
Christine Block

Christine Block QA, GCP

Clinical Pharmacology, Research and Clinical Research
Wilmington, Delaware, United States of America

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Christine has nearly 20 years of experience in clinical research, including 18 years of clinical quality assurance experience at small and large pharmaceutical companies as well as CROs. She joined Incyte Corporation in 2007 to establish and lead the Clinical QA-GCP function. In her current role at Incyte, she is responsible for developing and leading the QA-GCP audit program and has contributed to successful regulatory submissions and NDA approval of a new molecular entity. Prior to Incyte, Christine worked at AstraZeneca and Pfizer in various clinical QA roles of increasing responsibilities.

Christine has experience in various therapeutic areas, including but not limited to seven years in oncology and inflammation. She has extensive GCP knowledge and has FDA inspection experience at the site and sponsor level. Christine has been responsible for developing and conducting GCP training in her present and past positions and has conducted external training for other industry training organizations.

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