Margaret Lara
About Margaret Lara
Margaret Lara is a Clinical Trial Management Associate with over twenty years of experience in clinical research. She holds a Bachelor of Science from Texas A&M University - Corpus Christi and San Jose State University, and is certified as a Clinical Research Coordinator.
Work at Ardelyx
Margaret Lara currently serves as a Clinical Trial Management Associate at Ardelyx, Inc. She has been in this role since 2020. In her position, she applies her extensive knowledge of clinical research and regulatory guidelines to manage clinical trials effectively. Her responsibilities include ensuring compliance with Good Clinical Practice (GCP) and International Council for Harmonisation (ICH) guidelines, which are essential for maintaining the integrity of clinical studies.
Education and Expertise
Margaret Lara holds a Bachelor of Science degree in Health Science from San Jose State University, which she completed between 2010 and 2015. She also earned a Bachelor of Science from Texas A&M University - Corpus Christi. Additionally, she studied Medical Assisting at West Valley College, where she obtained an Associate of Science degree. Her educational background provides her with a solid foundation in health sciences, contributing to her expertise in clinical research.
Background in Clinical Research
Margaret Lara has over twenty years of experience in clinical research. She began her career as a Clinical Research Assistant at BD Biosciences from 2007 to 2012, where she gained foundational skills in the field. She continued to develop her expertise at ProTrials Research, where she worked as a Clinical Research Assistant and later as a QA Document Specialist. Her experience includes various roles at Pharmacyclics, an AbbVie Company, where she advanced from Clinical Development Coordinator to Senior Clinical Trial Assistant.
Certifications and Professional Skills
Margaret holds a Certified Clinical Research Coordinator (CCRC) certification from the Association of Clinical Research Professionals. This certification demonstrates her commitment to maintaining high standards in clinical research. She is recognized for her superior organizational skills and written communication abilities, which are critical for ensuring quality documentation in clinical trials. Her knowledge of industry guidelines further enhances her effectiveness in navigating the complexities of clinical research.