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Biography

Ms. Becker provides over 20 years of regulatory affairs and site management experience with a thorough knowledge of FDA guidelines, clinical trials operations, regulatory affairs, budget and analysis preparation, marketing, and new business procurement. Prior to joining аÄÃÅÁùºÏ²Ê¿ª½±Íø, Ms. Becker worked as Regulatory Affairs Specialist for Abrazo Community Health Network – Clinical and Translation Research Institute; her responsibilities included overseeing all regulatory aspects of Abrazo hospitals and facilities conducting both drug and medical device Phase II-IV clinical trials research. She has extensive experience with domestic and multinational research firms.

As the Clinical Research Services (CRS) Quality Assurance Specialist, she works closely with the Directors on both campuses. Her goal is to assure that studies being conducted by the CRS are in compliance with all applicable University policies, and Federal regulations concerning Clinical Research and the implementation of quality control procedures for assigned clinical trials conducted at the CRS.

Clinical Interests:

• Clinical Research Compliance
• Cardiovascular and Endovascular Research
• Women’s Health Research