Clinical Research Coordinator I

Kelly Services; Las Vegas (NV); On-site; USD 39,000 - 41,000; Full time

Job summary

Kelly Science & Clinical seeks a Clinical Research Coordinator for a contract opportunity in the Las Vegas area. This role supports day-to-day coordination of clinical studies, ensures compliance with GCP and regulatory requirements, and works closely with investigators, staff, and study participants.

The CRC will screen participants, obtain informed consent, schedule visits, collect data, and maintain study documentation while adhering to HIPAA, FDA regulations, and site SOPs.

Qualifications

• High school diploma or equivalent required.
• Associate’s degree or higher in a health-related field preferred.
• Experience with patient care and medical terminology is required.
• Prior clinical research experience or foundational knowledge is strongly preferred.

Responsibilities

• Coordinate and support clinical research studies per protocols and regulations.
• Screen potential participants and collect medical histories.
• Assist with informed consent and participant enrollment.
• Schedule visits, procedures, and follow-ups.
• Maintain accurate source documentation and data.
• Educate participants on study requirements and respond to questions.
• Monitor progress and report adverse events and deviations.
• Maintain study files and record management.
• Process laboratory specimens when qualified.
• Follow SOPs, HIPAA, GCP, FDA regulations, and other research standards.
• Support additional research activities as assigned.

Skills

Organizational skills

Communication

Microsoft Office

EDC systems

Education

High school diploma

Associate degree or higher in health-related field

Tools

Microsoft Office

Electronic Data Capture (EDC) systems

Job description

Clinical Research Coordinator
Location:Las Vegas, NV
Schedule:Monday–Friday | 8:00 AM – 5:00 PM
Pay Rate:$28.00–$30.00/hour
Job Type:Full-Time | Contract until EOY (can extend)

Kelly Science & Clinicalis seeking aClinical Research Coordinatorfor a contract opportunity with a clinical site network in the Las Vegas area. If you have experience supporting clinical trials, enjoy working directly with patients, and thrive in a fast-paced research environment, we’d love to hear from you.

Position Summary
The Clinical Research Coordinator (CRC) supports the day-to-day coordination and execution of clinical research studies while ensuring compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP) guidelines. This role partners closely with investigators, research staff, and study participants to ensure high-quality clinical research and an exceptional participant experience.

Responsibilities

• Coordinate and support clinical research studies in accordance with study protocols and regulatory requirements.
  
• Screen potential study participants and collect medical histories and other required information.
  
• Assist with the informed consent process and participant enrollment.
  
• Schedule study visits, procedures, and participant follow-up activities.
  
• Collect, document, and maintain accurate source documentation and clinical research data.
  
• Educate participants on study requirements and respond to study-related questions.
  
• Monitor study progress and report adverse events, protocol deviations, and other research-related findings.
  
• Maintain study files and documentation through scanning, uploading, filing, and record management.
  
• Draw, process, package, and ship laboratory specimens when qualified.
  
• Follow site SOPs, HIPAA, GCP, FDA regulations, and other applicable research standards.
  
• Support additional research activities as assigned.

Qualifications

• High school diploma or equivalent required; Associate’s degree or higher in a health-related field preferred.
  
• Previous clinical research experience or foundational knowledge of clinical research strongly preferred.
  
• Experience with patient care and medical terminology required.
  
• Strong organizational skills with the ability to manage multiple priorities and meet deadlines.
  
• Excellent communication and interpersonal skills.
  
• Proficiency with Microsoft Office and electronic data capture (EDC) systems preferred.
  
• Knowledge of GCP, HIPAA, ALCOA principles, FDA regulations, and IATA guidelines preferred.
  
• Experience with participant screening and informed consent is highly desirable.

Preferred Certifications

• Medical Assistant (MA) certification preferred.
  
• Current CPR/BLS certification preferred.
  
• Certified Clinical Research Coordinator (CCRC) certification, or willingness to obtain certification, preferred.

Why Kelly Science & Clinical?
At Kelly Science & Clinical, we connect talented professionals with industry-leading organizations advancing healthcare and scientific innovation. This contract opportunity offers the chance to gain valuable clinical research experience while working alongside a collaborative and dedicated research team.