Clinical Research Associate (CRA) - Neurology (Remote)

About the role

The Clinical Research Associate (CRA) – Neurology will manage assigned protocols and sites, ensuring compliance with ICH/GCP, company policies, and regulatory requirements. The role is remote with a preference for candidates located in the Southeast US.

Key responsibilities

• Develop strong site relationships and manage sites through all trial phases.
• Perform site monitoring (remote and on‑site) ensuring data completeness, accuracy and patient safety.
• Conduct site visits (validation, initiation, monitoring, close‑out) and document clear reports.
• Collect and review regulatory documentation for study start‑up, maintenance and close‑out.
• Identify and resolve site performance or compliance issues, escalating as needed.
• Maintain study information in CTMS, eTMF and other systems.
• Contribute to site identification and expansion in line with country strategy.

Required profile

• Associate’s degree or higher in a scientific/healthcare discipline with at least 5 years relevant experience, including 2 years site monitoring, or a Bachelor’s degree with at least 2 years monitoring experience.
• Experience in neurology clinical trials preferred.
• Ability to travel 65‑75% of time (≈2‑3 days/week) and hold a valid driver’s license.
• Fluency in English (verbal and written) and strong communication skills.
• Knowledge of ICH‑GCP, local regulations and Good Documentation Practices.

Required skills

• Clinical Site Management
• Clinical Study Management
• Clinical Trial Planning
• Clinical Trials Monitoring
• Data Reporting
• Good Clinical Data Management Practice (GCDMP)
• Neurology therapeutic area knowledge
• Remote Monitoring
• Site Management
• Use of MS Office and clinical IT applications (CTMS, eTMF)