Job Description

Position Overview:

Minneapolis Medical Institute is seeking an experienced Clinical Research Coordinator to join our team in executing cutting-edge Alzheimer’s clinical trials. This is a full-time, on-site position ideal for someone who is proactive, detail-oriented, and excited to grow within a fast-paced and meaningful research environment. You will be a key member of the site team, responsible for managing trial conduct from start to finish with full support from our centralized operations team.

Responsibilities

• Coordinate and conduct study visits in compliance with the study protocol, GCP, FDA, and IRB guidelines.
• Maintain accurate and timely documentation in source documents and electronic data capture (EDC) systems.
• Recruit, screen, enroll, and follow up with study participants.
• Prepare and maintain regulatory documents, logs, and case report forms.
• Communicate regularly with sponsors, CROs, monitors, and the internal study team.
• Manage investigational product handling, including IP accountability and temperature logs.
• Assist in resolving data queries and audit responses.
• Ensure proper documentation and handling of adverse events, deviations, and protocol changes.
• Participate in site initiation visits, monitor visits, closeout visits, and sponsor audits.

Qualifications

• Bachelor's degree in a healthcare or life sciences field preferred.
• Minimum of 2 years of experience as a Clinical Research Coordinator.
• Strong understanding of clinical trial processes, regulatory compliance, and subject safety.
• Experience with EDC systems, informed consent procedures, and protocol adherence.
• Strong organizational skills and excellent attention to detail.
• Ability to multitask and work independently in a fast-paced environment.
• Experience in Alzheimer’s or CNS research preferred but not required.

Benefits:

• Standard weekday schedule with no weekend responsibilities.
• Competitive salary and full benefits including health, dental, vision, 401(k), and paid time off (PTO).
• Full operational and administrative support provided by our corporate office—including study startup, regulatory submissions, budgets and contracts, recruitment, and closeout. CRCs may also attend investigator meetings for their designated studies—offering valuable exposure to sponsor relationships, protocol discussions, and professional networking opportunities.
• Professional development, training, and certification opportunities.

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