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Mark Arquiza

Mark Arquiza, MSc, CCRA

+1.802.488.0485 Visit Website
 

Mark Arquiza is an Associate Director, Clinical Monitoring Oversight, Apellis Pharmaceuticals, Inc. He has worked in the clinical research field for more than 20 years, gaining experiences in the specialties of clinical monitoring, quality oversight, line management, clinical trial management, project management, and vendor management. Mr. Arquiza’s dedication to clinical research is evident through his efforts in obtaining a Master of Science (with Merit) in Clinical Research from the University of Liverpool, his commitment in earning the Certified Clinical Research Associate (CCRA) designation from the Academy of Clinical Research Professionals, his industry publications, and his volunteer activities within the industry. Mr. Arquiza has also supervised Clinical Operations interns completing their summer and/or academic internships. Despite the travel requirements of his position, Mr. Arquiza still enjoys traveling in his off time to learn more about and to experience other cultures.

Specialties: Clinical Monitoring, Quality Management, Quality Oversight, Risk-Based Monitoring, Risk Management, Functional Services Provider (FSP), Good Clinical Practices (GCP/ICH E6), Line Management, Clinical Trial Management, Project Management, Vendor Management; Therapeutic Areas (Food Allergy, Haematology, and Oncology)