Clinical Research Coordinator

Elite Clinical Network; Las Vegas, Northern (NV, KY); Hybrid; USD 65,000 - 90,000; Full time

Job summary

Elite Clinical Network is seeking a highly organized Clinical Research Coordinator (CRC) to join our research team in Las Vegas, NV. The CRC will coordinate and support all aspects of clinical trials and research studies, including subject recruitment, data collection, regulatory compliance, and specimen handling.

Candidates with current Phlebotomy experience and certification are strongly preferred, as the role may include specimen collection and basic procedures.

Qualifications

• Bachelor's degree required.
• 4–5 years of CRC experience.
• Phlebotomy certification with experience.
• Knowlege of GCP and regulatory guidelines.
• Excellent organizational skills and attention to detail.
• Strong interpersonal and communication skills.
• Proficiency in Microsoft Office and REDCap/EDC systems.
• Ability to work independently and in a multidisciplinary team.

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.

Skills

GCP knowledge

Regulatory compliance

Data collection

Communication skills

Organizational skills

Education

Bachelor's degree in health-related field

Tools

REDCap

EDC platforms

Microsoft Office

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. Candidates with current Phlebotomy experience and certification are strongly preferred, as this role may include specimen collection and basic clinical procedures.

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.
• At least 4–5 years of experience as Clinical Research Coordinator.
• Phlebotomy certification with phlebotomy experience.
• 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:

• Phase I clinical trials experience is a definite a plus.
• Experience working in clinical trials, especially in a hospital or academic setting.
• Familiarity with IRB processes and clinical trial documentation.
• Bilingual skills (depending on patient population) may be a plus.