Clinical Research Coordinator – Onsite Study Coordination

TALENT Software Services; Rochester (MN); On-site; USD 52,000 - 68,000; Full time

Job summary

TALENT Software Services seeks a detail-oriented clinical research coordinator in Minnesota. This on-site role collaborates with investigators and staff, ensuring compliant execution of research protocols, participant interactions, and data management across multiple studies.

The position emphasizes regulatory duties, protocol development support, and coordination of study logistics with occasional travel. Strong attention to detail and customer-service experience are valued assets.

Qualifications

• One year of clinical research experience.
• Medical terminology course.
• Clinical research experience preferred; customer service or healthcare patient-facing experience accepted.
• Experience coordinating patient-facing activities, scheduling, documentation, and working within regulated environments is helpful.

Responsibilities

• Coordinates non-therapeutic clinical research protocols under PI or supervisor guidance in compliance with regulations.
• May assist in complex studies with direction but not overall responsibility.
• Screens, enrolls, and recruits research participants.
• Coordinates schedules and monitors research activities and subject participation.
• Recognizes adverse events and protocol deviations; reports appropriately and collects/enters data.
• Performs administrative and regulatory duties related to the study as assigned.
• Some travel may be required.
• Supports protocol development and maintenance activities (IRB submissions, study logistics, communications).
• Participates in other protocol development activities and executes other assignments as warranted.

Skills

Clinical research

Medical terminology

Patient scheduling

Documentation

Attention to detail

Job description

TALENT Software Services seeks a detail-oriented clinical research coordinator in Minnesota. This on-site role collaborates with investigators and staff, ensuring compliant execution of research protocols, participant interactions, and data management across multiple studies.

The position emphasizes regulatory duties, protocol development support, and coordination of study logistics with occasional travel. Strong attention to detail and customer-service experience are valued assets.