Clinical Research Coordinator

ECN Operating LLC; Las Vegas (NV); On-site; USD 65,000 - 90,000; Full time

Job summary

ECN Operating LLC is seeking a Clinical Research Coordinator (CRC) to join our research team in Las Vegas. 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 clinical procedures.

Qualifications

• Bachelor's degree in a health-related field is required.
• At least 4–5 years of experience as Clinical Research Coordinator.
• Phlebotomy certification with phlebotomy experience is strongly preferred.
• GCP knowledge and regulatory guidelines familiarity.
• Excellent organizational and attention-to-detail skills.
• Strong interpersonal and communication abilities.
• Proficiency in Microsoft Office and electronic data capture systems (REDCap, EDC).
• Ability to work independently and within 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 uphold ethical conduct in all interactions.
• Collect, process, and ship biological specimens per protocol (blood draws, urine samples).
• Perform basic clinical procedures as permitted by certification (vital signs, EKGs).
• Maintain accurate documentation in case report forms and electronic databases.
• Communicate with sponsors, monitors, and IRBs regarding 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

Clinical Research

GCP

Regulatory knowledge

Organizational skills

Communication skills

REDCap

EDC platforms

MS Office

Education

Bachelor's degree in health-related field

Phlebotomy certification

Tools

REDCap

EDC platforms

MS 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.