Research Nurse Specialist: Clinical Trials & Data Integrity

University of Miami; Miami (FL); On-site; USD 68,000 - 90,000; Full time

Job summary

The Nurse Specialist, Research at University of Miami ensures clinical studies comply with practice guidelines, regulations, and institutional policies while supporting participant recruitment and achievement of research objectives.

Key duties include data collection and entry from medical records, initiating visits, coordinating equipment, educating staff and participants on protocols and side effects, and monitoring adverse events.

Qualifications

• Bachelor’s degree in a relevant field.
• Valid Florida RN license.
• Certification in relevant specialty.
• Minimum 3 years of relevant experience.

Responsibilities

• Assess, troubleshoot, and report data collection problems to management.
• Identify desired research outcomes and monitor subjects’ responses.
• Conduct initiation visits and register patients in clinical studies.
• Perform study data collection and entry from charts and records.
• Identify and procure equipment and supplies needed for projects.
• Educate staff and subjects about protocols, treatment, possible side effects, and complications.
• Prepare and process new research proposals and amendments and monitor applications and adverse events.
• Assist with study closeout, data lock, and archiving of study files to ensure data completeness.
• Complete ongoing checks of clinical data on case report forms for accuracy and correction.
• Adhere to University policies and safeguard University assets.

Skills

Attention to detail

Prioritization

Confidentiality

Flexible hours

Teamwork

Integrity

Education

Bachelor’s degree in relevant field

Job description

The Nurse Specialist, Research at University of Miami ensures clinical studies comply with practice guidelines, regulations, and institutional policies while supporting participant recruitment and achievement of research objectives.

Key duties include data collection and entry from medical records, initiating visits, coordinating equipment, educating staff and participants on protocols and side effects, and monitoring adverse events.