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Full Time Pra Clinical Research Jobs in Springfield, MO

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Full Time Pra Clinical Research information

See Springfield, MO salary details

$44.6K

$97.6K

$171.9K

How much do full time pra clinical research jobs pay per year?

As of Sep 7, 2026, the average yearly pay for full time pra clinical research in Springfield, MO is $97,636.00, according to ZipRecruiter salary data. Most workers in this role earn between $73,700.00 and $111,400.00 per year, depending on experience, location, and employer.

What is the difference between Full Time Pra Clinical Research vs Clinical Research Coordinator?

AspectFull Time Pra Clinical ResearchClinical Research Coordinator
CredentialsBachelor's degree often required; certifications like CCRP beneficialBachelor's degree typically required; certifications like CCRP advantageous
Work EnvironmentResearch sites, hospitals, pharmaceutical companiesResearch sites, hospitals, clinics
Employer & IndustryPharmaceutical companies, CROs, research institutionsHospitals, clinics, research organizations

Both roles involve managing clinical trial activities, but Full Time Pra Clinical Research often focuses on supporting clinical research protocols and data collection, while Clinical Research Coordinators handle participant recruitment, scheduling, and compliance. The roles are similar in credentials and work environment, with differences mainly in specific responsibilities.

What are popular job titles related to Full Time Pra Clinical Research jobs in Springfield, MO?

For Full Time Pra Clinical Research jobs in Springfield, MO, the most frequently searched job titles are:

What job categories do people searching Full Time Pra Clinical Research jobs in Springfield, MO look for?

The top searched job categories for Full Time Pra Clinical Research jobs in Springfield, MO are:

What cities near Springfield, MO are hiring for Full Time Pra Clinical Research jobs?

Cities near Springfield, MO with the most Full Time Pra Clinical Research job openings:

Full Time Pra Clinical Research jobs near you
Infographic showing various Full Time Pra Clinical Research job openings in Springfield, MO as of August 2026, with employment types broken down into 3% As Needed, 71% Full Time, 18% Part Time, and 8% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $97,636 per year, or $46.9 per hour.

Clinical Research Coordinator

Headlands Research

Springfield, MO

$22 - $29.25/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 3 days ago

New

Job description

Clinical Research Coordinator (CRC)

Location: Springfield, MO | Site Name: Clinvest Research | Full-Time | Clinical Research

Are you an experienced clinical research professional with a passion for advancing medicine? Join a leading, integrated clinical research network dedicated to high-quality data, patient-centered care, and innovation in clinical trials.

We're seeking a Clinical Research Coordinator (CRC) for our clinical research site located in Springfield, MO. The CRC will manage and execute Phase I-IV clinical studies in accordance with FDA regulations, GCP/ICH guidelines, and sponsor protocols. This role is ideal for someone who thrives in a fast-paced environment and is eager to make an impact in the clinical research industry.

Type:  Regular Full-time Employee
Schedule:  Mondays through Thursdays 7:00am - 5:00pm; Fridays 7:00am - 12:00pm  NO NIGHTS!! NO WEEKENDS!! 
Location:  Onsite in Springfield, MO (no capabilities for remote or hybrid work)
Reports to:  Site Director
Benefits:  Our benefits package for full-time employees includes health insurance (medical, dental, and vision), Health Savings Accounts (HSA) and Flexible Spending Accounts (FSA), Paid Time Off (PTO), a variety of disability, accident, and life insurance options, as well as many more.

What We Offer
  • Competitive pay + annual performance incentives
  • Medical, dental, and vision insurance
  • 401(k) plan with company match
  • Paid time off (PTO) and company holidays
  • A mission-driven culture focused on advancing medicine and improving patient outcomes
 Why Join Us?

You'll be part of a growing, mission-driven organization that values its people. At our core, we're committed to bringing innovative medical treatments to patients faster-while creating an environment where employees thrive. If you're passionate about clinical research and ready to make a difference, we'd love to hear from you.

Responsibilities:

  • Coordinate all aspects of assigned clinical trials from site initiation to study close-out
  • Conduct subject visits and ensure timely, accurate documentation following ALCOA-C standards
  • Maintain compliance with study protocols, GCP/ICH guidelines, FDA regulations, IRB policies, and company SOPs
  • Manage subject recruitment, informed consent, and retention strategies
  • Ensure timely data entry and resolution of EDC queries
  • Report and follow up on all adverse events, serious adverse events, and deviations
  • Collaborate with investigators, lab teams, sponsors/CROs, and internal stakeholders
  • Prepare for and participate in monitoring visits, audits, and inspections
  • Maintain regulatory documentation and ensure proper training is completed for all study amendments and systems
  • Execute study procedures such as phlebotomy, ECGs, and sample processing within scope (as trained)
  • Attend investigator meetings and provide cross-functional support as needed
  • Maintain working knowledge of study protocols, laboratory manuals, equipment calibration, and inventory control

Requirements:

  • Bachelor's degree OR 2 years of college in a health-related program OR experience and training in conducting clinical trials with knowledge of ICH GCP
  • Previous experience as a Clinical Research Coordinator strongly preferred
  • Industry-sponsored trial experience strongly preferred (vaccine study experience a plus)
  • Familiarity with electronic data capture (EDC), IVRS, and other trial platforms
  • Deep understanding of FDA, ICH-GCP regulations, and clinical trial procedures
  • Proficiency in medical terminology and clinical documentation practices
  • Strong interpersonal, verbal, and written communication skills
  • Organized, detail-oriented, and capable of managing multiple priorities
  • Proficient in Microsoft Office and other clinical research systems

Apply