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.

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

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.

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 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.

Careers that change lives start here. Medtronic is a global leader in healthcare technology with a Mission to alleviate pain, restore health, and extend life. Our 95,000 employees work across more than 150 countries to put patients first — developing innovative medical technologies that improve the lives of 72+ million patients each year.

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

Responsible for managing the research activities at sites participating in Worldwide’s clinical research projects. Typically involved in all stages of the clinical study, including identifying potential sites to participate in the research effort, performing various study start-up activities such as working with sites to collect appropriate regulatory documents and supporting the negotiation of contracts and budgets, training the sites to collect data properly and report any potential safety-rel

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture.

Our FSP team is currently seeking a CRA 2 in West, Central, or South Regions with 2 years of monitoring! 8-10 days on site per month being a mix of onsite and remote.

As a Clinical Research Associate (CRA) at Worldwide, you will find yourself working alongside brilliant minds across diverse therapeutic areas, including Cardiovascular, Metabolic, Neuroscience, Oncology, and Rare Diseases. Collaboration with top-tier colleagues from various backgrounds and specialties is not just encouraged; it's ingrained in our culture.

As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation. You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.). Acting as a site processes specialist, you will ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' r

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.

Integrated Resources, Inc. seeks a Clinical Research Specialist to oversee center operations and ensure high-quality data collection. The specialist will act as the main liaison for assigned sites, coordinating with stakeholders to monitor performance, resolve discrepancies, and maintain compliance with regulatory standards.

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.