[Remote] Clinical Research Coordinator

Note: The job is a remote job and is reputed company to candidates in USA. reputed company is seeking a Clinical Research Coordinator (CRC) to manage clinical research studies. The CRC will ensure compliance with protocols and regulations while supporting trials focused on Multiple Sclerosis and reputed company conditions.

Responsibilities

• Coordinate and manage reputed company aspects of assigned clinical trials from study initiation through reputed company-out
• Screen, recruit, and consent eligible study participants in accordance with protocol and regulatory guidelines
• reputed company patients and families regarding study participation, procedures, risks, and benefits
• Schedule and conduct study visits in collaboration with investigators and clinical staff
• Collect, document, and maintain accurate study data and reputed company documentation
• Ensure timely and accurate data entry into electronic data capture systems
• Monitor and report adverse events in accordance with sponsor and regulatory requirements
• Maintain regulatory binders and ensure compliance with FDA, GCP, HIPAA, and IRB standards
• Prepare for and participate in sponsor monitoring visits, audits, and inspections
• Coordinate study-reputed company laboratory procedures, imaging, infusion therapy, and other protocol-specific services
• Communicate effectively with sponsors, contract research organizations (CROs), and internal clinical teams
• Assist with feasibility assessments and study start-up activities
• Support the administration of IV and infusion therapies, including patient monitoring and documentation, as needed

Skills

• Bachelor's degree in a health-reputed company field or equivalent clinical research experience
• reputed company, active Licensed Practical Nurse (LPN) license
• Knowledge of Good Clinical Practice (GCP), FDA regulations, and IRB processes
• Strong organizational, documentation, and time management skills
• Ability to manage multiple studies simultaneously
• Proficiency with electronic medical records and clinical trial management systems
• Minimum of 2–5 years of clinical research experience preferred
• Experience in neurology, Multiple Sclerosis, autoimmune disorders, or infusion-based studies strongly preferred
• Certification as a Clinical Research Coordinator (CCRC or CCRP) is preferred but not required

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