[Remote] Clinical Research Coordinator

Note: The job is a remote job and is open to candidates in USA. NextCode Placement specializes in connecting skilled professionals with leading organizations, helping bridge the gap between talent and opportunity. The Clinical Research Coordinator will manage day-to-day study activities, including participant recruitment, screening, informed consent, and scheduling of study visits while ensuring data integrity in accordance with study protocols and regulatory requirements.

Responsibilities

• Manage day-to-day study activities, including participant recruitment, screening, informed consent, and scheduling of study visits
• Maintaining accurate source documentation
• Completing case report forms
• Ensuring data integrity in accordance with study protocols and regulatory requirements
• Coordinating with investigators, clinical staff, sponsors, and institutional review boards
• Preparing and organizing study materials and reports
• Assisting with regulatory submissions
• Monitoring study timelines
• Supporting audit readiness
• Promoting adherence to Good Clinical Practice (GCP) and ethical standards

Skills

• Experience coordinating clinical research studies, including participant recruitment, informed consent, and visit management
• Strong skills in data collection, documentation, and electronic data entry, with attention to accuracy and confidentiality
• Knowledge of Good Clinical Practice (GCP), Institutional Review Board (IRB) processes, and applicable regulatory guidelines (e.g., FDA, HIPAA)
• Ability to collaborate effectively with investigators, clinical staff, sponsors, and external partners
• Excellent organizational and time-management abilities, with capacity to prioritize multiple studies and deadlines
• Clear, professional written and verbal communication skills for participant interaction and reporting
• Proficiency with standard office software and clinical research systems or electronic data capture platforms
• Bachelor's degree in a health-related, scientific, or social science field, or equivalent relevant experience
• Prior experience in clinical research, healthcare, or a related environment is preferred
• Certification as a Clinical Research Coordinator (e.g., ACRP, SOCRA) is a plus but not required

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