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Full Time Clinical Research Rater Jobs in Missouri

Washington University of St. Louis

$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 ...

Washington University of St. Louis

$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 ...

Washington University of St. Louis

$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 ...

ObjectiveHealth

Clinical Research Coordinator II

Columbia, MO · On-site

$23 - $30.75/hr

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

ObjectiveHealth

Clinical Research Coordinator I

Columbia, MO · On-site

$23 - $30.75/hr

Description 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 ...

ObjectiveHealth

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 ...

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Full Time Clinical Research Rater information

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 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 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 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 job categories do people searching Full Time Clinical Research Rater jobs in Missouri look for?

The top searched job categories for Full Time Clinical Research Rater jobs in Missouri 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:

Full Time Clinical Research Rater jobs near you
Infographic showing various Full Time Clinical Research Rater job openings in Missouri as of August 2026, with employment types broken down into 2% As Needed, 72% Full Time, 20% Part Time, and 6% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution.

Physician Assistant - Clinical Research

Headlands Research

Chesterfield, MO • On-site

Full-time

Re-posted 8 days ago

Job description

Championing Diversity in Clinical Trials

Diversity isn't just a checkbox for us - it's central to our mission. We're committed to advancing medical science by promoting diversity in every facet of clinical trial research. From our team composition to participant demographics, inclusivity is at the heart of everything we do.

The Role of a Lifetime

Are you ready to make a difference? We're seeking an experienced Nurse Practitioner or Physician Assistant to help us grow our clinical research site located in the Greater St. Louis Area. You will help the site conduct clinical research trials involving gastroenterology, neurology, vaccines, and general internal medicine.

Clinical Research Professionals (CRP) is a dedicated research center that provides a network of providers who work collaboratively in conducting clinical research trials. The site's team brings more than 20 years of experience, including many highly accomplished principal investigators across multiple therapeutic areas that are helping to improve lives through advancement of new drug therapies and medical devices.

Type:  Full-time Regular Employee 

Pay:  Competitive and dependent upon years of experience as an Investigator in clinical research. 

Location:  Onsite in Chesterfield, MO (no opportunities for remote or hybrid)

Schedule:  Mondays through Fridays, 8:00am-5:00pm

Responsibilities:

  • Ensure the safety and welfare of each study subject
  • Have in-depth knowledge of all research protocols
  • Screen potential study subjects according to the protocol's specific inclusion and exclusion criteria
  • Conduct medical history interviews and physical examinations throughout the subject's study participation
  • Review EKG's and lab results
  • Provide medical care as needed during a subject's participation in a clinical trial
  • Provide home based on-call availability per standard policy
  • Attend Investigator Meetings on behalf of Principal Investigator as needed
  • Excellent professional communication, punctual and responsible
  • Friendly and outgoing demeanor
  • Must demonstrate a passion for direct patient interaction
  • Demonstrate clinical competence, positive leadership and ability to work collaboratively with a multi-disciplinary team

Qualifications:

  • Minimum of two years of experience as a licensed family or non-acute adult nurse practitioner or physician assistant treating a wide variety of therapeutic areas for the adult and geriatric patient population required (internal medicine, family medicine, urgent care, emergency medicine)
  • Current and unencumbered license to practice as an NP or PA in the state of Missouri required
  • Prior experience within the clinical research industry required
  • Commitment and ability to deliver excellent customer service
  • Excellent communication, punctual and responsible
  • Extremely well organized
  • Excellent verbal and written communication skills
  • Trustworthy, reliable; attentive to details
  • Mature and pleasant demeanor
  • Willingness to learn new tasks and grow with the company

Apply