Sandra Chica, MD
About Sandra Chica, MD
Sandra Chica, MD, is the Director of Clinical Development in Immuno-Oncology at BeiGene, with over 10 years of experience in Oncology clinical development and extensive expertise in medical monitoring and regulatory strategy.
Title: Director, Clinical Development, Immuno-Oncology
Sandra Chica, MD, holds the position of Director of Clinical Development for Immuno-Oncology at BeiGene. In this role, she leverages her extensive experience in the field of Oncology to advance clinical trials and research initiatives. Her responsibilities encompass both strategic and tactical functions, such as clinical and regulatory strategy, protocol development, and data analysis and interpretation.
Previous Roles and Experience
Prior to her current role at BeiGene, Sandra Chica, MD, served as a Clinical Research Physician Consultant and Vice President for various organizations. She has held pivotal roles at entities such as Imaging Endpoints, BioTelemetry Research, and Novartis. Notably, she has also worked as a Senior Medical Director at Perceptive Informatics (PAREXEL), where she accumulated a wealth of experience in oncology clinical development.
Education and Radiology Training at CES University
Sandra Chica, MD, completed her medical education at CES University, formerly known as Instituto de Ciencias de la Salud. She earned her Medical Doctor degree after six years of study from 1988 to 1994. Subsequently, she pursued a Radiology Residency at the same institution, obtaining her Radiologist qualification after three additional years of study from 1996 to 1999.
Clinical Research and Oncology Focus
Sandra Chica, MD, has over a decade of experience specializing in oncology clinical development. Her work includes medical monitoring and safety support for clinical trials specifically targeting breast cancer, pancreatic cancer, and liver diseases such as NASH and cirrhosis. This diverse experience underpins her proficiency in developing relationships with clinical investigators and opinion leaders.
Expertise in Medical Writing and Regulatory Submissions
Sandra Chica, MD, possesses a robust background in medical writing and the preparation of regulatory documents and publications. She is adept at developing various study documents and facilitating activities related to regulatory submissions. Her expertise ensures the meticulous and accurate documentation required for successful clinical trial approvals.