Clinical Research Assistant - Data, Compliance & Participant Support

ECN Operating LLC; North Las Vegas (NV); On-site; USD 42,000 - 60,000; Full time

Job summary

ECN Operating LLC is seeking a Research Assistant to support clinical studies by performing administrative, technical, and participant-focused tasks under supervision. You will help ensure high-quality data collection, regulatory compliance, and participant safety in line with GCP and study protocols.

This role collaborates with the clinical team to facilitate study activities, maintain logs, assist with consent processes, and support site audits and ongoing education to stay current with

Qualifications

• Associate or bachelor’s degree in health sciences, biology, psychology, or related field.
• Prior healthcare or research experience preferred.
• Familiarity with clinical trials, GCP, HIPAA, and human subjects research regulations.
• Strong organizational, communication, and time management skills.
• Proficient with Microsoft Office and data entry systems; experience with EDC or CTMS is a plus.

Responsibilities

• Coordinate study materials, source documents, and regulatory binders.
• Support participant screening, scheduling, and enrollment tracking.
• Record data into eCRFs or databases accurately.
• Maintain confidentiality and HIPAA compliance.
• Assist in regulatory compliance and regulatory audits.
• Greet participants and assist during visits and consent processes.
• Collaborate with Clinical Research Coordinators and Principal Investigator.

Skills

Organizational skills

Communication skills

Time management

Education

Health sciences/biology/psychology degree

Tools

Microsoft Office

EDC

CTMS

Data entry systems

Job description

ECN Operating LLC is seeking a Research Assistant to support clinical studies by performing administrative, technical, and participant-focused tasks under supervision. You will help ensure high-quality data collection, regulatory compliance, and participant safety in line with GCP and study protocols.

This role collaborates with the clinical team to facilitate study activities, maintain logs, assist with consent processes, and support site audits and ongoing education to stay current with