Alison Jean Kolla

Alison Jean Kolla

Associate Director, Gcp Qa @ BeiGene

About Alison Jean Kolla

Alison Jean Kolla is the Associate Director of GCP QA at Beigene in Cambridge, Massachusetts, with over a decade of experience in clinical research and quality assurance.

Current Position

Alison Jean Kolla is the Associate Director of GCP QA at Beigene, based in Cambridge, Massachusetts, United States. Her role involves ensuring compliance with Good Clinical Practice (GCP) standards, focusing on maintaining the quality and integrity of clinical trials.

Professional Experience

Alison Jean Kolla has over a decade of experience in clinical research and quality assurance. She has held various roles in the industry, transitioning from Clinical Research Associate positions at PRA Health Sciences and Photothera to managerial roles at Medivation, Pfizer, and Beigene. Notably, she worked as a Study Manager at Pfizer and as a GCP Quality and Compliance Manager at Beigene before her current role. Her career spans across several high-profile companies in the pharmaceutical and biotechnology sectors.

Educational Background

Alison Jean Kolla studied Management and Design at the University of California, Santa Cruz (2008-2009). She earned her Bachelor's of Science degree from UC Santa Barbara, where she studied from 2004 to 2008. Her foundational education was completed at Singapore American School.

Geographic Experience

Throughout her career, Alison Jean Kolla has worked in diverse locations across the United States, including San Francisco, California; Raleigh, North Carolina; New York, New York; and Cambridge, Massachusetts. This geographical diversity has provided her with a broad understanding of regional regulatory environments and industry practices.

Career Progression

Alison Jean Kolla progressed rapidly in her career, moving from Clinical Research Associate roles to managerial positions within a span of three years. She has been involved in clinical trial management and quality assurance, leading initiatives to comply with GCP regulations. Her progression highlights her expertise and adaptability in clinical research.

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