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Full Time Clinical Research Rater Jobs in Missouri

$54K - $81K/yr

Lab/research equipment * Clinical/diagnostic equipment The above statements are intended to ... Individual rates within the range will be determined by factors including one's qualifications and ...

$54K - $81K/yr

Lab/research equipment * Clinical/diagnostic equipment The above statements are intended to ... Individual rates within the range will be determined by factors including one's qualifications and ...

$64K - $99K/yr

This person will oversee and coordinate complex or multi-site clinical research studies, serve as a ... Individual rates within the range will be determined by factors including one's qualifications and ...

$54K - $81K/yr

This full-time position plays an essential role in advancing our understanding of cerebrovascular ... Individual rates within the range will be determined by factors including one's qualifications and ...

Clinical Research Coordinator I

Saint Louis, MO · On-site

$22.75 - $30.25/hr

Clinical Research Coordinator I Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess ...

Clinical Research Coordinator I

Columbia, MO · On-site

$23 - $30.75/hr

Clinical Research Coordinator I Our clinical research company is looking to hire a qualified candidate for the full-time position of Clinical Research Coordinator. The ideal candidate will possess ...

$75K - $128K/yr

Monitors compliance of the clinical research division with the IRB, federal mandates and grant ... Individual rates within the range will be determined by factors including one's qualifications and ...

$58K - $90K/yr

Acts as the primary liaison to PI in developing plans for clinical research projects; collaborates ... Individual rates within the range will be determined by factors including one's qualifications and ...

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Full Time Clinical Research Rater information

Is a full time clinical research rater a good career?

A full-time clinical research rater is a role that involves evaluating clinical trial data, often requiring attention to detail and knowledge of medical terminology. It can offer stable employment and opportunities for growth in the healthcare and research industries, especially for those with relevant backgrounds or certifications. However, job satisfaction depends on individual interests and career goals in the clinical research field.

What are some typical challenges a full time clinical research rater may encounter, and how can they be managed?

Full Time Clinical Research Raters often face challenges such as managing large volumes of patient assessments, maintaining objectivity during subjective ratings, and adhering to strict study protocols. Balancing accuracy with efficiency is key, especially when dealing with sensitive patient information and tight study timelines. Collaborating closely with investigators and other research staff, participating in regular trainings, and using standardized rating tools can help ensure consistency and reliability in data collection.

What is the difference between Full Time Clinical Research Rater vs Part Time Clinical Research Rater?

AspectFull Time Clinical Research RaterPart Time Clinical Research Rater
Work HoursTypically 35-40 hours per weekLess than 20 hours per week
CertificationsOften requires relevant healthcare or research certificationsMay require similar certifications but less emphasis
Work EnvironmentFull-time employment in research facilities or remotePart-time roles, flexible locations
Employer UsageMajor research organizations, pharmaceutical companiesFreelance or contract research organizations

The main difference between a Full Time Clinical Research Rater and a Part Time Clinical Research Rater lies in work hours, certification emphasis, and employment type. Full-time roles offer consistent hours and benefits, while part-time positions provide flexibility. Both roles involve evaluating clinical data, but full-time positions are more integrated into research teams.

What are the key skills and qualifications needed to thrive as a full time clinical research rater?

Success as a Full Time Clinical Research Rater requires a background in psychology, neuroscience, or a related field, along with experience in clinical assessments and data collection. Familiarity with standardized rating scales, clinical trial databases, and regulatory compliance systems like Good Clinical Practice (GCP) certification is typically expected. Strong attention to detail, interpersonal communication, and objective judgment are crucial soft skills for accurate participant evaluation and collaboration with research teams. These competencies ensure reliable data collection, regulatory adherence, and the integrity of clinical research outcomes.

What is a full time clinical research rater?

Full Time Clinical Research Raters are professionals who assess and document the progress, symptoms, and responses of patients participating in clinical research studies. They use standardized rating scales, interviews, and questionnaires to collect accurate data that helps determine the effectiveness and safety of new treatments or interventions. These raters play a vital role in ensuring the integrity and quality of clinical trial data, often working closely with clinicians, researchers, and study coordinators. Their responsibilities also include adhering to study protocols, maintaining patient confidentiality, and ensuring compliance with regulatory standards.
What are the most commonly searched types of Clinical Research Rater jobs in Missouri? The most popular types of Clinical Research Rater jobs in Missouri are:
What are popular job titles related to Full Time Clinical Research Rater jobs in Missouri? For Full Time Clinical Research Rater jobs in Missouri, the most frequently searched job titles are:
What cities in Missouri are hiring for Full Time Clinical Research Rater jobs? Cities in Missouri with the most Full Time Clinical Research Rater job openings:
Infographic showing various Full Time Clinical Research Rater job openings in Missouri as of August 2026, with employment types broken down into 100% Full Time. Highlights an 100% In-person job distribution.

Research Assistant / Patient Recruitment

Headlands Research

Chesterfield, MO

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Re-posted 24 days ago


Job description

Clinical Research Assistant / Patient Recruitment Assistant

Location: Chesterfield, MO  Site Name: Clinical Research Professionals | Full-Time | Clinical Research

We're seeking a Clinical Research Assistant (RA) / Patient Recruitment Specialist for our Clinical Research Professionals site located in Chesterfield, MO. As an RA, you won't just be supporting research-you'll be helping shape the future of healthcare. This is an exciting opportunity for individuals with clinical experience who are ready to grow their skillset and income potential within the clinical research field.

The Role:

As a Clinical Research Assistant, you'll work side-by-side with experienced Clinical Research Coordinators, Investigators, and cross-functional teams to support all aspects of clinical trial execution-from subject screening, data entry, to patient recruitment. Your work will directly contribute to the success of new treatments in development.

Type:  Regular Full-time Employee 
Schedule:  Mondays through Fridays, 8:00am - 4:00pm
Location:  Onsite in Chesterfield, MO (no capabilities for remote or hybrid work)
Reports to:  Clinical Manager
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
  • Opportunities for professional development and career growth
  • A mission-driven culture focused on advancing medicine and improving patient outcomes

Responsibilities:

  • Assist research coordinators in conducting clinical trial visits in compliance with study protocols
  • Make outbound phone calls to recruit patients for upcoming trials
  • Collect and record vital signs, make study-related phone calls, and document data in electronic systems
  • Support subject screening, enrollment, and follow-up processes
  • Review and verify study documentation for accuracy and completeness
  • Maintain close communication with coordinators, investigators, and study participants

Requirements:

  • Familiarity with medical terminology and basic laboratory procedures preferred
  • Prior experience providing direct hands-on patient care preferred
  • You must be comfortable sometimes spending long hours on the phone speaking with potential clinical trial participants
  • Clinical research experience preferred
  • Comfortable using multiple electronic data entry systems
  • Strong attention to detail, time management, and ability to work in a fast-paced, regulated environment
  • Excellent interpersonal skills-you'll be interacting with participants, providers, and sponsors
  • Passion for improving patient outcomes through research