Senior Clinical Research Coordinator – Neurology (Contract)

Senior Clinical Research Coordinator – Neurology (Contract)

About the Role

We’re hiring a Senior Clinical Research Coordinator (SCRC) to support Neurology clinical trials. This role focuses on executing complex studies with a strong emphasis on protocol compliance, patient management, and data quality.

You’ll play a key role in coordinating all aspects of clinical trials while working closely with investigators, sponsors, and research teams.

Assignment Details

• Schedule: Monday–Friday | 8:30 AM – 5:00 PM
• Duration: 15-week contract
• Work Setting: Fully on-site
• Pay Range: $32–$43/hour

Key Responsibilities

• Oversee daily coordination of Neurology clinical trials across multiple phases
• Manage patient screening, recruitment, consent, enrollment, and follow-up visits
• Ensure compliance with study protocols, GCP, IRB, FDA, and HIPAA guidelines
• Maintain study documentation, regulatory files, and electronic records (CTMS/e-reg)
• Perform data collection, entry, and review, ensuring completeness and accuracy
• Coordinate study visits, monitoring activities, and sponsor communications
• Work closely with investigators, CROs, and internal departments to execute studies
• Support early-phase and interventional trials, maintaining strict protocol adherence
• Assist with audit readiness and regulatory inspections
• Contribute to training and mentorship of junior staff

Requirements

• Bachelor’s degree and 4+ years of clinical research experience
• (or equivalent combination of education and experience)
• Strong knowledge of clinical trial operations, GCP, IRB, and FDA regulations
• Experience using CTMS and clinical research data systems
• Ability to manage multiple studies in a fast-paced environment

Preferred Background

• Experience in Neurology clinical research
• Exposure to interventional or early-phase trials
• Background in pediatric or hospital-based research environments
• Experience in high-enrollment study settings

Core Skills

• Neurology Clinical Research (Interventional & Multi-Phase Trials)
• GCP & Regulatory Compliance (IRB, FDA, HIPAA)
• Study Coordination & Protocol Execution
• Patient Recruitment & Study Visit Management
• Clinical Data Management & CTMS Systems