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Sarah Al-Gassimi has a diverse work experience in the field of biotechnology and research. Sarah began their career at Johns Hopkins Aramco Healthcare as an intern, where they gained experience in various laboratory techniques and clinical laboratory work.

Sarah then worked as a Research Assistant at Florida Institute of Technology, where they performed laboratory techniques such as protein and DNA extraction, western blot, and agarose gel electrophoresis. Sarah also managed laboratory purchasing and inventory processes.

Sarah then joined Morphogenesis, Inc. as a Production Associate, where they successfully performed upstream production, downstream production, and aseptic fill-finish processes. Sarah ensured compliance with the company's Quality Management System.

Sarah later took on the role of Production Manager, overseeing biologics production. Sarah was responsible for managing operational processes, equipment, and documentation. Sarah collaborated with various departments to meet objectives and comply with regulations.

Most recently, Sarah has been a Clinical Research Associate at Morphogenesis, Inc. Here, they have been responsible for trial management, including trial design, feasibility, regulatory compliance, and data management. Sarah also handles clinical operations responsibilities such as IRB submissions, GCP compliance, CRO/CRA management, and trial logistics. Additionally, they support interactions with CMOs, CRO partners, and clinical sites.

Overall, Sarah Al-Gassimi has gained experience in laboratory techniques, biologics production, and clinical research, showcasing their adaptability and knowledge in the biotechnology sector.

Sarah Al-Gassimi completed their Bachelor's degree in Clinical Laboratory Science/Medical Technology/Technologist from Imam Abdulrahman Bin Faisal University from 2008 to 2012. Sarah then pursued a Master's degree in Biotechnology from Florida Institute of Technology from 2015 to 2017. Additionally, Sarah obtained various certifications, including Process Improvement: Identifying and Eliminating Waste at Work and Home, Designated Project Manager, USF Lean Six Sigma Yellow Belt Certification, Achieving Data Quality and Integrity in Clinical Trials Involving High Consequence Pathogens, Interpretation and Application of ICH E6(R2), Advanced Clinical Research Associate Certification (ACRAC), Good Clinical Practices (cGCP), Good Documentation Practices, Good Manufacturing Practices (cGMP), and Process Validation. These certifications were obtained from institutions such as USF Corporate Training and Professional Education, University of Nebraska Medical Center, Multi-Regional Clinical Trials Center of Brigham and Women's Hospital and Harvard (MRCT Center), CCRPS, and Learnaboutgmp. The certifications were earned between 2021 and 2023.