Clinical Research Coordinator

Elite Clinical Network; Henderson (NV); On-site; USD 55,000 - 85,000; Full time

Job summary

Elite Clinical Network seeks a highly organized Clinical Research Coordinator to support all aspects of clinical trials, including recruitment, data collection, regulatory compliance, and specimen handling.

The CRC will coordinate day-to-day activities, obtain informed consent, manage specimens, and perform basic clinical procedures while maintaining meticulous documentation in CRFs and EDC systems.

Qualifications

• Bachelor’s degree in a health-related field is required.
• Minimum 3 years of experience as a Clinical Research Coordinator.
• Phlebotomy experience and certification.
• Knowledge of GCP and regulatory guidelines.
• Excellent organizational and attention to detail.
• Strong interpersonal and communication skills.
• Proficiency with Microsoft Office and REDCap/EDC systems.
• Ability to work independently and in a multidisciplinary team.

Responsibilities

• Coordinate day-to-day clinical research activities per study protocols.
• Recruit, screen, and enroll study participants.
• Obtain informed consent and ensure ethical conduct.
• Handle specimens per protocol (blood/urine).
• Perform basic procedures (vital signs, EKGs) as certified.
• Maintain accurate documentation in CRFs and EDC databases.
• Communicate with sponsors, monitors, and IRBs regarding study progress.
• Schedule participant visits and ensure visit windows are met.
• Maintain regulatory documents and assist IRB submissions.

Skills

Organizational skills

Interpersonal communication

Microsoft Office

REDCap

EDC systems

Team collaboration

Education

Bachelor's degree in health-related field

Tools

REDCap

Microsoft Office

EDC platforms

Job description

We are seeking a highly organized and motivated Clinical Research Coordinator (CRC) to join our research team. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling.

Key Responsibilities

• Coordinate day‑to‑day clinical research activities to ensure study protocols are followed.
• Recruit, screen, and enroll study participants.
• Obtain informed consent and ensure ethical conduct in all study interactions.
• Collect, process, and ship biological specimens per protocol (e.g., blood draws, urine samples).
• Perform basic clinical procedures as permitted by certification (e.g., vital signs, EKGs).
• Maintain accurate and timely documentation in case report forms and electronic databases.
• Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
• Schedule participant visits and follow‑ups; ensure visit windows are met.
• Ensure proper storage, handling, and accountability of investigational products, if applicable.
• Maintain regulatory documents and assist with IRB submissions.

Qualifications

• Bachelor's degree in a health‑related field required.
• 3 years of experience as a Clinical Research Coordinator.
• Phlebotomy experience and certification.
• Knowledge of Good Clinical Practice (GCP) and regulatory guidelines.
• Excellent organizational skills and attention to detail.
• Strong interpersonal and communication skills.
• Proficiency in Microsoft Office and electronic data capture systems (e.g., REDCap, EDC platforms).
• Ability to work independently and as part of a multidisciplinary team.

Preferred Qualifications

• Experience working in Pulmonary clinical trials.
• Familiarity with IRB processes and clinical trial documentation.
• Bilingual skills (depending on patient population) may be a plus.