Tara Mcclellan

Mrs. Tara McClellan is an essential member of the Antria team with over 10 years in the research industry. Mrs. McClellan has vast experience working as both a Clinical Research Coordinator and Clinical Research Associate (monitor) with experience in all clinical trial phases (I-IV) for various indications. Her focus as a monitor is in the management and oversight of the clinical trial. She understands that timelines are important, and monitoring must be done in the most efficient and effective manner possible. As a monitor, she ensures compliance with FDA-approved clinical research protocols, and that data is protected and verified to maintain scientific integrity. Her goal is to protect patients' rights, safety, and well-being throughout the study. She maintains certification in Good Clinical Practice (GCP), IATA Dangerous Goods, and CPR.