Clinical Research Associate Jobs in Minnesota, United States

Clinical Research team at Inspire Medical Systems conducts innovative sleep apnea device trials. The Clinical Research Associate II oversees site initiation, training, and monitoring to ensure protocol compliance and data quality, performing both remote and on‑site visits.

Clinical Operations at Worldwide Clinical Trials drives multi‑therapeutic clinical studies. The Senior Clinical Research Associate manages site activities, conducts initiation visits, ensures regulatory compliance, and trains sites on data collection, all while supporting safety reporting.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical studies across therapeutic areas. As a Senior Clinical Research Associate, you will manage site activities, conduct initiation visits, and ensure regulatory compliance for CNS trials, primarily working remotely with regional travel.

Cancer and Blood Disorders Clinical Research team at Children’s Minnesota supports pediatric oncology and hematology studies. The Clinical Research Associate I assists with study startup, data entry, regulatory submissions, and patient coordination, ensuring compliance with GCP and IRB standards.

Clinical Operations at Worldwide Clinical Trials drives innovative clinical research across therapeutic areas. The Senior Clinical Research Associate manages site activities for CNS and Rare Disease studies, conducts initiation visits, ensures regulatory compliance, and supports data collection remotely while traveling regionally as needed.

Division of Behavioral Medicine and Clinical Psychology at Cincinnati Children’s Hospital Medical Center seeks a Research Associate/Full Professor to lead an independent, externally funded program focused on internalizing disorders such as anxiety, depression, and suicide. The role involves securing and managing grant funding, conducting high-impact research on health disparities in pediatric mental health, and collaborating with the Mental and Behavioral Health Institute.

The Associate Clinical Research Coordinator at Mayo Clinic's Comprehensive Cancer Center coordinates non-therapeutic clinical research protocols under the direction of a principal investigator or supervisor, ensuring compliance with regulatory laws and institutional guidelines. Day-to-day duties include screening, enrolling, and recruiting research participants; coordinating schedules and monitoring research activities; recognizing and reporting adverse events, protocol deviations, and unanticip

Mayo Clinic Clinical Research team conducts Alzheimer's disease studies to advance patient care. The Clinical Research Coordinator independently manages complex interventional protocols, recruits participants, oversees data quality, and ensures regulatory compliance.

Mayo Clinic Research team focuses on advancing Alzheimer's disease studies through rigorous clinical protocols and data management. The Clinical Research Assistant supports study coordination, patient scheduling, data entry, and compliance with federal and sponsor guidelines, working closely with investigators and lab staff.

Heart & Vascular Center at CentraCare Health System conducts cutting‑edge cardiovascular research. As a Clinical Research RN you will screen and enroll patients, coordinate care, and manage study protocols alongside physicians and industry sponsors.

Mayo Clinic Clinical Research team advances Alzheimer's disease studies by coordinating complex interventional protocols and ensuring regulatory compliance. The Clinical Research Coordinator independently manages protocol development, participant recruitment, neuropsychometric testing, and data quality while collaborating with investigators and study sites.

Heart Center Research at CentraCare Health System drives innovative cardiovascular studies. The Clinical Research Coordinator manages project timelines, regulatory submissions, and stakeholder communication to ensure successful study execution.

A contract Clinical Research Specialist will manage study enrollment, maintain trial files, audit compliance, track device accountability, analyze deviations, prepare reports, coordinate meetings, and report status to management.

Clinical Research Specialist III – a senior role focused on ensuring regulatory compliance and audit readiness for a pre‑market application (PMA) submission. The specialist reviews Trial Master Files and site documentation to confirm adherence to ISO 14155, FDA regulations, and internal SOPs.

Senior Clinical Research Monitor oversees investigational site compliance, ensuring adherence to regulatory standards, IRB protocols, and study plans. The role conducts site visits, documents findings, and collaborates with investigators to resolve deviations.