Keywords: Senior Clinical Research Associate, Senior CRA, Clinical Research Associate, CNS Clinical Trials, Neurology Trials, Neuroscience Research, Cardiovascular Clinical Trials, Cardiology Studies, Phase II Clinical Trials, Phase III Clinical Trials, Clinical Monitoring, Independent Monitoring, Site Monitoring, Site Management, Clinical Operations, ICH-GCP, FDA Regulations, GCP Compliance, Clinical Trial Management, Source Data Verification, SDV, Source Data Review, SDR, CRF Review, Case Report Forms, Site Initiation Visits, SIV, Interim Monitoring Visits, IMV, Closeout Visits, COV, Investigative Sites, Patient Enrollment, Subject Recruitment, Clinical Development, Site Oversight, Risk Management, Protocol Compliance, Regulatory Compliance, Data Quality, Inspection Readiness, Sponsor-Facing, CRO, Biotechnology, Pharmaceutical Research, Clinical Study Management, Trial Execution, Clinical Research Operations, Monitoring Visits, Neurology, CNS Disorders, Epilepsy, Parkinson's Disease, Alzheimer's Disease, Multiple Sclerosis, Stroke, Cardiovascular Research, Heart Failure, Hypertension, Coronary Artery Disease, Arrhythmia Studies, Clinical Research Monitoring. This is a full time opportunity that requires regional travel and can be located anywhere in the U.S. Responsibilities for the Senior Clinical Research Associate include: Independently monitoring Phase II-III CNS and Cardiovascular clinical trials to ensure compliance with study protocols, ICH-GCP guidelines, and regulatory requirements.