Contract Clinical Research Assistant

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

Job summary

Kelly Science & Clinical is seeking a Clinical Research Coordinator in Las Vegas, NV to support day-to-day coordination of clinical studies and ensure GCP/HIPAA compliance. The CRC will work with investigators, staff, and participants to provide high-quality research and a positive participant experience.

The role emphasizes patient interaction, study coordination, data documentation, and adherence to SOPs and regulatory standards in a fast-paced environment.

Qualifications

• High school diploma or equivalent required; Associate degree preferred.
• Clinical research experience or foundational knowledge preferred.
• Experience with patient care and medical terminology required.
• Strong organizational and communication skills.
• Proficiency with Microsoft Office and EDC systems preferred.
• Knowledge of GCP, HIPAA, FDA regulations, and IATA guidelines preferred.
• CCRC or MA certification preferred.

Responsibilities

• Coordinate and support clinical research studies per protocols and regulatory requirements.
• Screen potential study participants and collect medical histories.
• Assist with informed consent and participant enrollment.
• Schedule study visits, procedures, and follow-ups.
• Maintain accurate study documentation and data provenance.
• Educate participants on study requirements and address questions.
• Monitor progress and report adverse events or protocol deviations.
• Maintain and organize study files and records.

Skills

Organizational skills

Communication skills

Microsoft Office

EDC systems

GCP knowledge

HIPAA knowledge

Patient interaction

Education

High school diploma

Associate degree or higher

Tools

Microsoft Office

EDC systems

Job description

Clinical Research Coordinator

Location:Las Vegas, NV
Schedule:Monday–Friday | Business Hours |
Pay Rate:$28.00 – $30.00/hour
Job Type:Full-Time | Now until 1/2027. This opportunity could be extended past the end of the year and has the potential for a CRC to convert to a permanent employee based on the site needs

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. If you have experience supporting clinical trials, enjoy working directly with patients, and thrive in a fast-paced research environment.

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.