Clinical Research Specialist

Job Summary and Responsibilities As our Clinical Research Specialist professional, you will be instrumental in advancing medical knowledge by expertly managing and executing clinical trials. You will ensure the highest standards of data integrity, patient safety, and regulatory compliance throughout the research process. Every day you will manage trial activities, including participant recruitment, data collection, and documentation, serving as a key liaison for all stakeholders. You will ensure strict adherence to protocols and regulatory requirements from study initiation to completion. To be successful in this role, you will bring relevant clinical research experience and a strong understanding of regulatory guidelines (e.g., GCP, FDA). Your exceptional organizational skills, attention to detail, and ability to communicate effectively will be crucial in this dynamic field. Coordinates and schedules subject study visits to ensure adequate supplies, procedures and investigator availability. Provides study specific, individualized education to study subjects and families. Ensures all appropriate subject consents are obtained. Collects and processes protocol required specimens. Acts as a liaison between Sponsor, Investigator, and Study Subject Collects all required study data and completes CRFs in a timely, accurate manner. Job Requirements Required Associates Degree in related field or an equivalent combination of relevant education and job‑related experience in lieu of a degree Minimum Two (2) years related experience Preferred Bachelors Degree in related field Three (3)+ years clinical experience Location Saint Joseph’s Hospital and Medical Center (SJHMC), Phoenix AZ #J-18808-Ljbffr