Remote CRA II: Clinical Monitoring & Data

NCBioImpact; Durham (NC); Hybride; USD 65 000 - 72 000; Plein temps

Résumé du poste

Fortrea is seeking an In-House Clinical Research Associate II to support clinical project teams in executing research studies. The role involves on-site or home-based activities, travel for site visits, and collaboration with the study team to ensure data quality and regulatory compliance.

Responsibilities include coordinating with investigative sites, monitoring site performance, aiding in patient recruitment, and preparing for visits.

Qualifications

• Requires basic understanding of ICH-GCP guidelines.
• Requires knowledge of clinical trials process and local regulatory requirements.
• Proven ability to work within a matrix team and coordinate with multiple stakeholders.

Responsabilités

• Serve as contact for project team and sites; document and report site interactions.
• Monitor site performance and implement action plans to meet expectations.
• Assist with recruitment activities and tracking; discuss risks with project management.
• Prepare for site visits, run reports, QC files, and resolve action items from visits.
• Ensure compliance with regulatory requirements and study budgets; support CTL and Project Manager.

Connaissances

Communication skills

Problem solving

Time management

Formation

Bachelor’s degree in biological or life sciences

Description du poste

Fortrea is seeking an In-House Clinical Research Associate II to support clinical project teams in executing research studies. The role involves on-site or home-based activities, travel for site visits, and collaboration with the study team to ensure data quality and regulatory compliance.

Responsibilities include coordinating with investigative sites, monitoring site performance, aiding in patient recruitment, and preparing for visits.