Clinical Research Associate Jobs in Minnesota, United States

FSP Clinical Research Team conducts oncology trials to advance cancer therapies. The CRA monitors study sites, conducts pre‑study and initiation visits, ensures protocol compliance, reviews CRFs, reports serious adverse events, and supports site staff.

Clinical Research Associate II on the PPD Development team at Thermo Fisher Scientific, driving clinical monitoring and site management for oncology and ophthalmology trials. The role conducts remote and on‑site visits, applies risk‑based monitoring, ensures protocol compliance, and collaborates with investigators to maintain audit readiness.

Clinical Research Associate at NAMSA supports medical device studies by ensuring GCP compliance, coordinating site monitoring, conducting qualification and close‑out visits, serving as primary contact for site queries, communicating performance trends, supporting study start‑up and document quality, providing training, maintaining master files, tracking enrollment and adverse events, attending meetings, reporting progress, supporting safety activities, and preparing regulatory submissions.

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.

Clinical Operations at Worldwide Clinical Trials drives innovative oncology studies across the Central United States. The Senior Clinical Research Associate manages site activities from start-up through close-out, conducts initiation visits, ensures regulatory compliance, and supports data collection and safety reporting.

Clinical Operations at Worldwide Clinical Trials drives multi‑therapeutic clinical studies, delivering end‑to‑end site management and regulatory oversight. The Senior CRA will manage research activities across sites, conduct study initiation visits, ensure compliance with consent and safety reporting, and support contract and budget negotiations while primarily working remotely across the Central United States.

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.

Cranial & Spinal Technologies (CST) at Medtronic builds integrated surgical solutions for spine and cranial conditions. The Associate Clinical Research Specialist supports post‑market clinical trials, managing site training, data quality, and regulatory compliance across the U.S. Remote within the Upper Midwest, the role requires occasional travel to investigative sites and a valid driver’s license.

Antibody Validation Group | Customer Applications | R&D at Bio-Techne focuses on advancing antibody validation strategies to support cutting‑edge research and clinical diagnostics. The Senior Research Associate leads IHC workflow development, designs validation studies, and applies computational image analysis tools to generate actionable insights, while mentoring junior staff and collaborating cross‑functionally with R&D and product teams.

Clinical Operations at AXIS CLINICALS LLC focuses on executing rigorous clinical studies. The Research Associate I assists with screening, vital sign collection, ECGs, and sample processing to support pharmacokinetic and vasoconstriction trials.

Luminex Operations at Bio-Techne builds made‑to‑order multiplex assays that enable researchers to study diseases critical for drug discovery and clinical trials. The Advanced Research Associate formulates assay cocktails, qualifies components, troubleshoots assays, maintains equipment, and manages batch records to ensure rapid, high‑quality turnaround.

Luminex Operations at Bio-Techne builds made‑to‑order Luminex Multiplexing Assays that enable researchers to study diseases critical for drug discovery and clinical studies. The Advanced Research Associate supports manufacturing processes, formulates microparticle and biotin cocktails, troubleshoots assays, drafts change plans, and maintains equipment and batch records.

By joining Bio-Techne, you’ll join a company with a powerful and positive purpose of enabling cutting-edge research in Life Sciences and Clinical Diagnostics. Bio-Techne, and all of its brands, provides tools for researchers to further treat and prevent disease worldwide.

Clinical Research Specialist at Allina Health supports clinical trials at Mercy Hospital. Responsibilities include study feasibility assessment, protocol evaluation, regulatory document preparation, patient enrollment, informed consent, data entry, and coordination with IRB and sponsors.

Allina Health, a not‑for‑profit health system serving Minnesota and western Wisconsin, seeks a Clinical Research Specialist to support clinical trials at Abbott Northwestern Hospital. The role involves patient enrollment, assessments, data management, and study material preparation.

Clinical Research Specialist role at Allina Health supports clinical trials at Abbott Northwestern Hospital. Responsibilities include study feasibility assessment, protocol evaluation, equipment ordering, radiology and imaging capability assessment, site qualification visits, recruitment strategy development, regulatory document preparation, informed consent administration, data entry into case report forms, source documentation management, and coordination with investigators, sponsors, and clinical teams.

Allina Health, a not-for-profit health system serving Minnesota and western Wisconsin, seeks a Clinical Research Specialist to support clinical trials. The role involves patient enrollment, data management, regulatory documentation, and coordination with IRB and sponsors.

Research Associate II supports clinic operations, manages patient care workflows, performs clinical procedures, data entry, ensures regulatory compliance, and trains staff. Works in Richfield office, Monday-Friday, 5 days.

The University of Minnesota Clinical Research Unit (CRU) is a premier facility embedded within the University of Minnesota Health system, supporting cutting‑edge medical studies. The RN Clinic Specialist will provide nursing care in the CRU’s Clinical Research Clinic at 516 Delaware St. SE, Minneapolis, MN. Responsibilities include assessing patient needs, coordinating care with the health‑care team, implementing nursing interventions per care plans, and delivering care as delegated by physicians.