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New · posted Nov 1

IQVIA · Pharmaceuticals

Clinical Research Coordinator

  • Jefferson City, MO
  • On-site
  • Part-time
  • Associate & Specialist
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EmploymentPart-time
DeadlineOpen until filled

The role

We are seeking a Clinical Research Coordinator (CRC) to join our team and support clinical research studies under the supervision of a principal investigator. This role involves hands-on clinical procedures, community outreach, and ensuring the highest standards of care and compliance.

Clinical Research Coordinator – Jefferson City, MO

Work Set-Up: On-site Schedule Weekly Hours: 24 hours/week

What you need

  • Bachelor’s degree preferred or equivalent combination of education and relevant experience.

  • Minimum 1+ years of relevant work experience in clinical research.

  • Working knowledge of clinical trials, GCP principles, and medical terminology.

  • Strong attention to detail and ability to establish effective working relationships.

  • Proficiency with EDC systems, data entry accuracy, and query management.

Please note: This position is not eligible for sponsorship.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What you'll do

  • Perform a variety of clinical procedures, including ECG, sample collection, and vital signs.

  • Coordinate clinical research studies and maintain compliance with protocols and Good Clinical Practice (GCP) guidelines.

  • Support study conducts by preparing study materials, setting up equipment, and planning logistical activities.

  • Recruit, screen, and orient patients, ensuring their safety and well-being throughout the study.

  • Collect and accurately record clinical data in case report forms (CRFs).

  • Collaborate with investigators and monitors, addressing queries and ensuring data quality.

  • Act as a patient advocate and maintain a safe environment in accordance with Health and Safety policies.

Pay

$72,800 – $87,360 a year

Employer provided

$35.00 – $42.00 an hour · yearly at 2,080 hours (40 a week)

How this compares

Where you'll work

Jefferson City, MOOn-siteOpen in Maps (opens in a new tab)

More jobs in Jefferson City, MO
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From the posting

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our team combines deep scientific expertise with cutting-edge technology to deliver high-quality data and insights that shape the future of clinical trials.

IQVIA company page · 83 open roles
Equal opportunity, accessibility and legal noticesIQVIA's statements, word for word

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

Job intelligence

The context around this role

Live data · November 1, 2026

Salary intelligence

How the pay compares

This role's midpoint is 27% below the US median for Clinical Research roles at this level.

This roleEmployer provided

$72,800 to $87,360 a year

Associate & Specialist roles in the US56 roles publishing pay

Middle half $80,000 to $127,875, median $110,000
Annual base pay
Annual base payLowMedianHigh
This role$72,800—$87,360
All US$80,000$110,000$127,875

This role: IQVIA's own published range, converted to a year at 2,080 hours. Comparisons: the base pay employers published on open Clinical Research roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Research

The general path across 193 open Clinical Research roles on Regulatory Jobs, with the titles they carry most. Not IQVIA's own promotion track.

  1. This role

    Associate & Specialist

    Often: Clinical Research Associate · Clinical Research Coordinator

    $110K median102 open
  2. Next step

    Senior & Principal

    Often: Senior Clinical Research Associate · Sr. CRA

    $125K median87 open
  3. Later

    Manager

    Often: Associate Clinical Research Manager · Senior Clinical Research Manager

  4. Later

    Director

    Often: Associate Director, Site Monitoring · Director, Clinical Trial Liaison

Skills DNA

What this role leans on

How many of the posting's 18 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 3 linesLab testing and methods: 1 lineDocumentation and SOPs: 3 linesInvestigations and CAPA: 2 linesValidation and qualification: 1 lineData and digital systems: 1 lineClinical trial conduct: 7 linesCollaboration and leadership: 2 linesGMPLab testingDocumentationInvestigationsValidationData systemsClinical trialsTeamwork
  • Clinical trial conduct7
  • GMP and compliance3
  • Documentation and SOPs3
  • Investigations and CAPA2
  • Collaboration and leadership2
  • Lab testing and methods1
  • Validation and qualification1
  • Data and digital systems1

Regulatory intelligence

The rules behind this role

Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.

Company hiring pulse

IQVIA on Regulatory Jobs

83
Open roles
59
Distinct roles
26
Locations

By discipline

  • Clinical72 87%
  • Regulatory7 8%
  • Quality4 5%

By level

  • Associate & Specialist43 52%
  • Manager15 18%
  • Senior & Principal15 18%
See all 83 IQVIA roles

More roles at IQVIA

All 83 IQVIA roles

Similar Clinical Research roles elsewhere

Clinical Research Coordinator at IQVIA

Open until filled. $73K–$87K a year, employer provided.

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