Pediatric Clinical Research Coordinator (Hybrid)

University of Minnesota; Minneapolis (MN); Hybrid; USD 55,000 - 70,000; Full time

Job summary

The University of Minnesota is seeking a Clinical Research Coordinator to support pediatric clinical studies, manage participant enrollment, and ensure regulatory compliance. The role involves coordinating visits, data collection, specimen handling, and contributing to publications.

Responsibilities include adverse event reporting, regulatory binder maintenance, and collaboration with PI and study team. Hybrid work arrangement with opportunities for professional growth and impact on patient care.

Qualifications

• BA/BS in a scientific or health related field and 2 years research experience OR a combination of education and experience in research to equal 6 years
• Experience as a research coordinator in clinical research, including obtaining informed consent
• Working knowledge of Good Clinical Practices (GCPs), and federal regulations related to clinical research
• Experience with computerized data management, preferably in a health-related setting and including experience with electronic medical records
• Detail-oriented with exceptional organizational, planning and problem-solving skills
• Ability to work independently, as a part of a team and with changing priorities
• Demonstrated ability to maintain deadlines and prioritize assignments
• Excellent written, verbal and interpersonal skills
• During a typical 8 hour shift, standing/walking requirements

Responsibilities

• Coordinate patient participation in clinical research, including screening and recruiting patients and families, ensuring study eligibility and enrollment, scheduling and conducting research visits
• Data collection and submission for multiple projects, engaging with providers and investigators for source documentation and data recording
• Specimen management for multiple projects including collection, processing, and shipment of research specimens
• Facilitate timely review and reporting of adverse reactions and serious adverse events
• Contribute to the production of research publications or presentations of research data
• Support regulatory submissions and maintain required documentation to ensure compliance
• Assist in study startup activities and mentor other coordinators
• Communicate with clinical teams to foster quality research participation

Skills

Informed consent

GCPs knowledge

Data management

Electronic Medical Records

Team collaboration

Education

BA/BS in science or health field

Tools

Electronic Medical Records

Data management software

Job description

The University of Minnesota is seeking a Clinical Research Coordinator to support pediatric clinical studies, manage participant enrollment, and ensure regulatory compliance. The role involves coordinating visits, data collection, specimen handling, and contributing to publications.

Responsibilities include adverse event reporting, regulatory binder maintenance, and collaboration with PI and study team. Hybrid work arrangement with opportunities for professional growth and impact on patient care.