Clinical Research Coordinator

ECN Operating LLC; Henderson (NV); On-site; USD 55,000 - 75,000; Full time

Job summary

ECN Operating LLC in Henderson, NV is seeking a Clinical Research Coordinator to oversee and support clinical trials, including participant recruitment, data collection, regulatory compliance, and specimen handling.

The ideal candidate holds a bachelor's degree in a health-related field, at least 3 years as a CRC, phlebotomy certification, and solid knowledge of GCP and electronic data capture systems such as REDCap.

Qualifications

• Bachelor's degree in a health-related field required.
• At least 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 (REDCap, EDC).
• Ability to work independently and as part of a multidisciplinary team.

Responsibilities

• Coordinate day-to-day clinical research activities to ensure protocol adherence.
• Recruit, screen, and enroll study participants.
• Obtain informed consent and ensure ethical conduct in all interactions.
• Collect, process, and ship biological specimens per protocol.
• Perform basic clinical procedures as certified (e.g., vital signs, EKGs).
• Maintain accurate documentation in case report forms and electronic databases.
• Communicate with sponsors, monitors, and IRBs regarding study progress and compliance.
• Schedule participant visits and 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

Organizational skills

Communication skills

Independent worker

Teamwork

Attention to detail

Education

Bachelor's degree in health-related field

Tools

REDCap

EDC platforms

Microsoft Office

Job description

Clinical Research Coordinator (CRC)

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 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.