Research Registered Nurse

NEUROLOGY CONSULTANTS OF DALLAS P A • Irving, TX

6d

About The Position

The Research Registered Nurse (RN) provides clinical, administrative, and operational leadership for clinical trials conducted in outpatient clinic and hospital settings. This role is responsible for performing protocol-required clinical procedures, overseeing multi-site study execution, ensuring regulatory compliance, supervising research personnel, and managing study-related financial processes. The Research RN plays a critical role in maintaining study integrity, participant safety, regulatory compliance, and operational efficiency.

Requirements

• Active, unrestricted Registered Nurse (RN) license
• Minimum 3 years of clinical nursing experience, including infusion therapy
• Clinical research experience required
• Strong working knowledge of GCP, regulatory requirements, and clinical trial financial management

Nice To Haves

• Bachelor of Science in Nursing (BSN) preferred

Responsibilities

• Clinical Trial Implementation
• Perform protocol-specific procedures, including IV placement, infusions, injections, and fluid administration
• Prepare, handle, and administer investigational products in accordance with protocol and safety standards
• Monitor participants for adverse events and ensure appropriate documentation and follow-up
• Conduct clinical assessments and support protocol-driven evaluations
• Provide participant education and ensure adherence to study requirements
• Administrative, Regulatory & Financial Management
• Maintain essential regulatory documents, study binders, and source documentation
• Ensure compliance with GCP, IRB requirements, sponsor protocols, and institutional policies
• Coordinate study start-up, amendments, continuing reviews, and close-out processes
• Maintain investigational product accountability and study supply records
• Track enrollment, study milestones, and reporting requirements
• Manage study-related billing and invoicing, including preparation, reconciliation, and coordination with sponsors and finance departments to ensure accurate and timely payment
• Multi-Site & Operational Oversight
• Oversee day-to-day study operations across outpatient and hospital-based sites
• Ensure consistent protocol implementation and quality standards across locations
• Coordinate scheduling, staffing, and resource allocation to meet study timelines
• Serve as primary liaison with investigators, sponsors, CROs, monitors, and institutional departments
• Lead preparation for monitoring visits, audits, and inspections
• Personnel Leadership
• Supervise and mentor research coordinators, nursing staff, and support personnel
• Train staff on study protocols, clinical procedures, and compliance standards
• Delegate responsibilities and monitor performance and workflow efficiency
• Evaluate staff performance and implement process improvements to enhance productivity and compliance

What This Job Offers

• Job Type: Full-time
• Career Level: Mid Level